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<h2 class="h5">Job description</h2>
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<br> Company culture : <p><strong>Cnexia</strong> is driven by a culture strongly focused on <strong>performance and competitiveness</strong>, where ambition, challenge and customer orientation are key drivers of success. This dynamic is complemented by a <strong>collaborative dimension</strong>, promoting trust, teamwork and close managerial support. It also integrates an <strong>innovation component</strong> that encourages initiative, adaptability and experimentation. Finally, a structured <strong>organizational culture</strong> underpins the whole by ensuring process rigor, reliability and operational efficiency.
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<br> Job : <p>- Participate in conducting hiring interviews and annual medical consultations with the occupational physician.<br>- Ensure the creation, management, and updating of medical records for all company employees.<br>- Manage the medical service.<br>- Participate in prevention, health, hygiene, and safety education initiatives.<br>- Diagnose work-related accidents and provide first aid within your scope of responsibility.<br>- Ensure the availability of all medical equipment (medications, etc.) necessary for employee safety.<br>- Oversee the safety and health of employees.<br>- Comply with hygiene and safety rules according to the internal hygiene and safety policy.<br>- Receive and submit health insurance files to the insurance company contacts.<br>- Prepare a weekly report specifying the status of health file reimbursements.<br>- Prepare a weekly report including the number of women on maternity leave and individuals on long-term sick leave.<br>- Produce a monthly report differentiating between short-term and long-term sick leave.<br>- Track monthly data on employees with recurring absences.<br>- Ensure the accuracy of employee medical information.<br>- Comply with group policies and procedures regarding safety. </p><br><br> <br> <br> Required profile : <p>- Nursing diploma: State or Red Crescent nurse.<br>- Proficiency in computer tools: Word, Excel.<br>- Basic knowledge of Moroccan labor legislation regarding hygiene and safety.<br>- Discretion, organization, sociability, good communication, excellent interpersonal skills with employees.</p><br><br> <br><br> </div>
<p>ROLE PURPOSE: Promotion of Aspen products to healthcare professionals in a certain territory of the Moroccan Kingdom, including building relations with HCPs, delivering the brand marketing messages, achieving sales targets and participating in local/international events.</p><p>RESPONSIBILITIES: Represent Aspen by achieving daily targeted calls to physicians and pharmacists. Conducting AVAs & promotional activities Achieve sales budget in the designated territory. Build sustainable positive relationships with target HCPs and different stakeholders. Maintain an updated customer database Keeping up to date with the latest clinical data in the related therapy area, presenting and discussing this data with health professionals. Monitoring competitors, staying informed about competitors activities in a defined area. Organising appointments and meetings with community- and hospital-based healthcare staff Introduce ASPEN products in the hospital tender nomenclature Demonstrating or presenting products to healthcare staff, including doctors, nurses and pharmacists Undertaking relevant field research Meeting both the business and scientific needs of healthcare professionals Maintaining detailed records Attending and organising trade exhibitions, conferences and meetings Managing budgets and reviewing sales performance Writing reports and other documents</p><p>What we look for in candidates At Aspen, our culture is built on core values that drive our success and foster a supportive, innovative environment. We value Teamwork, where diverse perspectives and skills come together to enhance creativity and problem-solving. Innovation is at our core, as we continually seek better ways to achieve our goals and remain at the forefront of our industry. We demonstrate Commitment by exceeding expectations and building long-term relationships, while always striving for Excellence in everything we do. Our foundation of Integrity ensures that honesty, ethical behavior, and accountability guide our decisions. By proceeding with this job application, we understand that you share these values, and we look forward to reviewing your application and engaging with you further.</p><p><strong>Desired Candidate Profile</strong></p><ul><li>Master's in Pharmacy or/and Scientific Background (Not Mandatory)</li><li>Three (0-3) years as Medical Representative, Key Account Manager or Similar</li><li>One (1) year - preferably in Pharmaceuticals</li><li>MS Office - Working knowledge</li><li>CRM / Call Report - Working knowledge</li><li>Market Knowledge</li><li>Flexibility and tolerance for ambiguity</li><li>Technical /Professional skills</li><li>Consumer relevancy</li><li>Capacity for and resistance to stress</li><li>Industry knowledge</li><li>Problem solving</li><li>Active listening</li><li>Curiosity/learning agility</li><li>Information seeking</li><li>Informal communication skills</li><li>BUSINESS Foster Consumer & Customer Commitment Makes Good Decision</li><li>PEOPLE Communicate Effectively Dealing with ambiguity/Embrace change</li><li>SELF Continuously Grow & Develop Contribute Special Expertise</li></ul>
<p><strong>Description</strong></p><p>Promotion of Aspen products to healthcare professionals in a certain territory of the Moroccan Kingdom, including building relations with HCPs, delivering the brand marketing messages, achieving sales targets and participating in local/international events.</p><p><strong>RESPONSIBILITIES:</strong></p><ul><li>Represent Aspen by achieving daily targeted calls to physicians and pharmacists.</li><li>Conducting AVAs & promotional activities</li><li>Achieve sales budget in the designated territory.</li><li>Build sustainable positive relationships with target HCPs and different stakeholders.</li><li>Maintain an updated customer database</li><li>Keeping up to date with the latest clinical data in the related therapy area, presenting and discussing this data with health professionals.</li><li>Monitoring competitors, staying informed about competitors activities in a defined area.</li><li>Organising appointments and meetings with community- and hospital-based healthcare staff</li><li>Introduce ASPEN products in the hospital tender nomenclature</li><li>Demonstrating or presenting products to healthcare staff, including doctors, nurses and pharmacists</li><li>Undertaking relevant field research</li><li>Meeting both the business and scientific needs of healthcare professionals</li><li>Maintaining detailed records</li><li>Attending and organising trade exhibitions, conferences and meetings</li><li>Managing budgets and reviewing sales performance</li><li>Writing reports and other documents</li></ul><p>What we look for in candidates</p><p>At Aspen, our culture is built on core values that drive our success and foster a supportive, innovative environment. We value Teamwork, where diverse perspectives and skills come together to enhance creativity and problem-solving. Innovation is at our core, as we continually seek better ways to achieve our goals and remain at the forefront of our industry. We demonstrate Commitment by exceeding expectations and building long-term relationships, while always striving for Excellence in everything we do. Our foundation of Integrity ensures that honesty, ethical behavior, and accountability guide our decisions. By proceeding with this job application, we understand that you share these values, and we look forward to reviewing your application and engaging with you further.</p><p><strong>Requirements</strong></p><p><strong>EDUCATION QUALIFICATIONS AND EXPERIENCE:</strong></p><ul><li>Master's in Pharmacy or/and Scientific Background (Not Mandatory)</li><li>Three (0-3) years as Medical Representative, Key Account Manager or Similar</li><li>One (1) year - preferably in Pharmaceuticals</li></ul><p><strong>TECHNICAL SKILLS:</strong></p><ul><li>MS Office - Working knowledge</li><li>CRM / Call Report - Working knowledge</li></ul><p><strong>KEY ATTRIBUTES:</strong></p><ul><li>Market Knowledge</li><li>Flexibility and tolerance for ambiguity</li><li>Technical /Professional skills</li><li>Consumer relevancy</li><li>Capacity for and resistance to stress</li><li>Industry knowledge</li><li>Problem solving</li><li>Active listening</li><li>Curiosity/learning agility</li><li>Information seeking</li><li>Informal communication skills</li></ul><p><strong>ASPEN COMPETENCIES:</strong></p><ul><li>BUSINESS Foster Consumer & Customer Commitment Makes Good Decision</li><li>PEOPLE Communicate Effectively Dealing with ambiguity/Embrace change</li><li>SELF Continuously Grow & Develop Contribute Special Expertise</li></ul><p><br></p><p><strong>Desired Candidate Profile</strong></p><ul><li>Master's in Pharmacy or/and Scientific Background (Not Mandatory)</li><li>Three (0-3) years as Medical Representative, Key Account Manager or Similar</li><li>One (1) year - preferably in Pharmaceuticals</li><li>MS Office - Working knowledge</li><li>CRM / Call Report - Working knowledge</li><li>Market Knowledge</li><li>Flexibility and tolerance for ambiguity</li><li>Technical /Professional skills</li><li>Consumer relevancy</li><li>Capacity for and resistance to stress</li><li>Industry knowledge</li><li>Problem solving</li><li>Active listening</li><li>Curiosity/learning agility</li><li>Information seeking</li><li>Informal communication skills</li><li>BUSINESS Foster Consumer & Customer Commitment Makes Good Decision</li><li>PEOPLE Communicate Effectively Dealing with ambiguity/Embrace change</li><li>SELF Continuously Grow & Develop Contribute Special Expertise</li></ul>
<h2 class="h5">Job description</h2>
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<span></span><p><b>Join Yazaki. Connect to the future. </b></p><br> <p><b>Country</b>: Morocco (MA) <br>
<b>City</b>: Tangier<br>
<b>Worksite / Location</b>: Tanger Plant </p><br> <p><b>Job Function</b>: CEO_EHS & Sustainability <br>
<b>Job Discipline</b>: <br>
<b>Job Family</b>: Administrative Services</p><br> <p>Founded in 1929, Yazaki is a Japanese full systems supplier of wire harness, electrical, data products and solutions enabling vehicle electrification, connectivity, and autonomy integration. More than 235,000 committed and highly motivated employees in 45 countries make us one of the most successful international automotive suppliers. Join a family-owned company committed to being environmentally friendly in every aspect of its business, contributing to society, and inspiring trust. To strengthen our team, we are looking for a Nurse in our plant in [[location]].</p><br>
<p><strong>Key Responsibilities:</strong></p><br>
<p>• Provide first aid and emergency medical care to employees.</p><br>
<p>• Conduct health assessments and monitor employee wellness.</p><br>
<p>• Maintain medical records and occupational health documentation.</p><br>
<p>• Support workplace health and safety initiatives.</p><br>
<p>• Assist with medical examinations and return-to-work programs.</p><br>
<p><strong>Qualifications:</strong></p><br>
<p>✔ Bac+Diploma in Nursing.</p><br>
<p>✔ Strong communication, and interpersonal skills.</p><br>
<p>✔ Commitment to patient safety and quality care.</p><br>
<p>✔ 3years experience.</p><br><p>At Yazaki, we are committed to providing equal employment opportunities for everyone which extends to all aspects of the employment relationship. </p><br> <p>We are looking forward to receiving your application and to get to know you. Please apply by clicking the 'Apply Now' button. We wish you all the success in your application! </p><br> <p>Ps. Didn't find what you are looking for?<br> Take a look at our careers page! Be careful though, you might find your next dream job. </p><br>
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<h2 class="h5">Job description</h2>
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<span></span><p><b>Join Yazaki. Connect to the future. </b></p><br> <p><b>Country</b>: Morocco (MA) <br>
<b>City</b>: Tangier<br>
<b>Worksite / Location</b>: Tangier Logistics Hub </p><br> <p><b>Job Function</b>: People & CA_EHS & Sustainability <br>
<b>Job Discipline</b>: <br>
<b>Job Family</b>: Administrative Services</p><br> <p>Founded in 1929, Yazaki is a Japanese full systems supplier of wire harness, electrical, data products and solutions enabling vehicle electrification, connectivity, and autonomy integration. More than 235,000 committed and highly motivated employees in 45 countries make us one of the most successful international automotive suppliers. Join a family-owned company committed to being environmentally friendly in every aspect of its business, contributing to society, and inspiring trust. To strengthen our team, we are looking for a Nurse in our plant in [[location]].</p><br>
<p><strong>Key Responsibilities:</strong></p><br>
<p>• Provide first aid and emergency medical care to employees.</p><br>
<p>• Conduct health assessments and monitor employee wellness.</p><br>
<p>• Maintain medical records and occupational health documentation.</p><br>
<p>• Support workplace health and safety initiatives.</p><br>
<p>• Assist with medical examinations and return-to-work programs.</p><br>
<p><strong>Qualifications:</strong></p><br>
<p>✔ Bac+Diploma in Nursing.</p><br>
<p>✔ Strong communication, and interpersonal skills.</p><br>
<p>✔ Commitment to patient safety and quality care.</p><br>
<p>✔ 3years experience.</p><br><p>At Yazaki, we are committed to providing equal employment opportunities for everyone which extends to all aspects of the employment relationship. </p><br> <p>We are looking forward to receiving your application and to get to know you. Please apply by clicking the 'Apply Now' button. We wish you all the success in your application! </p><br> <p>Ps. Didn't find what you are looking for?<br> Take a look at our careers page! Be careful though, you might find your next dream job. </p><br>
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<h2 class="h5">Job description</h2>
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Job : <p>As part of strengthening the team of our partner, a company specialized in the industrial sector, we are recruiting an Occupational Health Nurse M/F.</p><br><br><p>The main goal of this position is to monitor the health of employees and contribute to the prevention of occupational risks, in a stimulating industrial environment where your rigor, organizational skills, and expertise will be major assets.</p><br><br><p><strong>Main Missions</strong></p><br><br><ul><li>Provide basic medical care to employees;</li><li>Monitor the health status of employees;</li><li>Participate in the prevention of occupational risks: musculoskeletal disorders, chemicals, heat, noise, etc.;</li><li>Participate in workplace safety and prevention actions;</li><li>Ensure that employee medical records are kept up to date and monitor health insurance;</li><li>Educate employees on first aid, ergonomics, and prevention;</li><li>Participate in awareness and prevention actions regarding occupational health and safety.</li></ul> <br> Required profile : <ul><li><strong>Diploma of General Nurse</strong> recognized by the <strong>Ministry of Health and Social Protection</strong>;</li><li>Experience in an industrial environment is preferred;</li><li>Knowledge of <strong>Hygiene</strong>, <strong>Safety</strong>, and <strong>Environment</strong> (HSE) is appreciated;</li><li>A qualification in industrial first aid or SST is an asset;</li><li>Knowledge in managing work stress and psychosocial risks is appreciated;</li><li>Knowledge in industrial toxicology is a plus;</li><li>Rigor, organization, reactivity, and sense of responsibility.</li></ul><p><strong>Conditions</strong></p><br><br><ul><li>Contract: Temporary</li><li>Salary: Negotiable depending on profile and experience</li><li>Transport: Provided in the Mohammedia areas</li></ul><br><p>Interested candidates are invited to send their CV to:<strong> mohammedia@groupe-crit.com</strong></p><br><br><p><strong>Subject: Application - Occupational Health Nurse M/F</strong></p><br><br><br><p>We look forward to hearing from you and good luck to all candidates!</p><br><br> <br><br> </div>
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<p><i><b>Join AstraZeneca, be part of a mission that puts patients first and be the driving force behind impactful healthcare solutions! If you're passionate about science, strategic in your approach, and thrive on building meaningful relationships with healthcare professionals — this is your chance to grow with a global leader and make a difference where it truly matters.</b></i></p><br><p><b>ABOUT ASTRAZENECA</b></p><br><p>AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.</p><br><p>Join a high-performing team, empowered to cut through the noise and drive real change. Our agility and pace, coupled with scientific focus, powers us to spot opportunities in the market that keep us moving forward and into new spaces.</p><br><p> <b>Why AstraZeneca?</b></p><br><p>At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.</p><br><p><b>ABOUT THE ROLE</b></p><br><p><b>Job Purpose:</b></p><br><p>As a Senior Medical Representative, your primary role is to drive product awareness and adoption by engaging healthcare professionals with scientific, ethical, and impactful communication—supporting AstraZeneca’s mission to improve patient outcomes and achieve business goals within the assigned territory.</p><br><p><b>Key Responsibilities:</b></p><br><p>• Collaborate with sales managers to develop and implement effective territory sales plans.</p><br><p>• Drive sales performance by meeting or surpassing sales forecasts and managing assigned budgets effectively to fulfil therapeutic and territorial objectives.</p><br><p>• Apply AstraZeneca’s marketing and medical promotion strategies across assigned regions and products.</p><br><p>• Conduct regular, high-quality medical visits to promote products and increase awareness among healthcare professionals about the company’s products, their indications, and clinical benefits, aligned with an approved visits plan and tailored visit objectives.</p><br><p>• Maintain up-to-date records of interactions, activities, and doctor profiles using CRM tools (e.g., Veeva).</p><br><p>• Organize and manage promotional meetings (RLM, ROM) and ensure efficient budget use for promotional activities.</p><br><p>• Deliver personalized, scientifically accurate messages aligned with physicians’ needs and prescribing behaviour.</p><br><p>• Monitor competitor activity and local market dynamics to inform promotional strategy and optimize positioning.</p><br><p>• Coordinate with internal departments for medical information, pharmacovigilance, and marketing feedback.</p><br><p>• Maintain strong, ethical relationships with healthcare professionals and uphold AstraZeneca’s professional values.</p><br><p>• Continuously develop product and therapeutic knowledge through company training and self-learning.</p><br><p>• Maintain comprehensive knowledge of the market, demographics, and managed care information relevant to the assigned territory to optimize sales strategies.</p><br><p>• Adhere strictly to all industry regulations and company policies regarding interactions with healthcare professionals, including the distribution of product samples.</p><br><p><b>Job Requirements:</b></p><br><p><b><u>Essential Criteria:</u></b></p><br><ul><li>Bachelor’s degree in Pharmacy, Medicine, Life Sciences, or a related field.</li><li>Minimum 2 -5 years as a Medical Representative in the pharmaceutical industry, Cardiovascular or respiratory background experience is mandatory.</li><li>for Internal Candidates :candidate must hold the position of medical representative and have achieved 2 consecutive years of strong performance with in AstraZeneca</li><li>Proven ability to thrive in a collaborative team environment.</li><li>Demonstrates strong cross-functional collaboration skills by working effectively with colleagues across departments such as Marketing, Medical, Regulatory, and Market Access to ensure alignment, share knowledge, and drive cohesive business strategies.</li><li>Strong knowledge of medical promotion practices, ethical guidelines, and local healthcare regulations.</li><li>Ability to analyse sales data (e.g., IMS), identify opportunities, and implement targeted action plans.</li><li>Excellent communication and interpersonal skills, with the ability to build and maintain professional relationships with healthcare professionals.</li><li>Proficient in CRM tools (e.g., Veeva) and daily reporting procedures.</li><li>Strong planning and organizational skills with the ability to manage territory visits, events, and budgets effectively.</li><li>Comfortable working in a dynamic, fast-paced environment and capable of adapting to changes quickly and professionally.</li><li>Commitment to continuous learning, with a proactive approach to maintaining up-to-date product and market knowledge.</li></ul><p>• Proficiency in both French and Arabic is required. English Command is a huge asset</p><br><br><p><i><b>Please note that this position is based in Morocco and is not open for relocation; only apply if you are located in or can easily access this location.</b></i></p><br><p><b>Date Posted</b></p><br>27-Oct-2026<p><b>Closing Date</b></p><br>02-Nov-2026<p>AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.</p><br> </div>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution<br>of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill<br>strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and<br>personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial<br>oversight to staff members, including performance assessment, training and feedback, resolution of personnel issues, and management of talent retention.</p><br><p><br>Responsibilities :</p><br><ul><li>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</li><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul><br>Qualifications<br><br><ul><li>Minimum of Bachelor’s Degree required. PhD, PharmD, Master’s Degree preferred. Relevant professional certification/credential (eg, CMPP, AMWA) is a plus.</li><li>4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg, medical communication agency) experience required</li><li>Demonstrated abilities in a leadership capacity required</li><li>Ability to understand and interpret medical data require</li><li>Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required</li><li>Knowledge of clinical/scientific publication structure, content, and quality. Knowledge of scientific publication regulations and best practices</li><li>Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences</li><li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record</li><li>Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise</li><li>Microsoft Office and Internet navigation proficiencies essential</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our long-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution<br>of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill<br>strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and<br>personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial<br>oversight to staff members, including performance assessment, training and feedback, resolution of personnel issues, and management of talent retention.</p><br><p><br>Responsibilities :</p><br><ul><li>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</li><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul><br>Qualifications<br><br><ul><li>Minimum of Bachelor’s Degree required. PhD, PharmD, Master’s Degree preferred. Relevant professional certification/credential (eg, CMPP, AMWA) is a plus.</li><li>4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg, medical communication agency) experience required</li><li>Demonstrated abilities in a leadership capacity required</li><li>Ability to understand and interpret medical data require</li><li>Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required</li><li>Knowledge of clinical/scientific publication structure, content, and quality. Knowledge of scientific publication regulations and best practices</li><li>Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences</li><li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record</li><li>Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise</li><li>Microsoft Office and Internet navigation proficiencies essential</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our long-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution<br>of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill<br>strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and<br>personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial<br>oversight to staff members, including performance assessment, training and feedback, resolution of personnel issues, and management of talent retention.</p><br><p><br>Responsibilities :</p><br><ul><li>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</li><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul><br>Qualifications<br><br><ul><li>Minimum of Bachelor’s Degree required. PhD, PharmD, Master’s Degree preferred. Relevant professional certification/credential (eg, CMPP, AMWA) is a plus.</li><li>4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg, medical communication agency) experience required</li><li>Demonstrated abilities in a leadership capacity required</li><li>Ability to understand and interpret medical data require</li><li>Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required</li><li>Knowledge of clinical/scientific publication structure, content, and quality. Knowledge of scientific publication regulations and best practices</li><li>Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences</li><li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record</li><li>Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise</li><li>Microsoft Office and Internet navigation proficiencies essential</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our long-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Seeking a results-driven and technically oriented MES Recipe Author within our pharmaceutical operation, reporting into the Digital Systems organization. The MES Recipe Author plays an important role in developing, validating, and maintaining electronic batch records and recipes within MES platform, POMSnet. This position is responsible for authoring recipes and supporting change control activities in alignment with quality standards and GMP regulations.</p><br><p><strong>Responsibilities:</strong></p><br><ul><li>Author, configure, and verify master batch records (MBRs), templates, and electronic batch records (EBRs) using MES platforms (e.g., POMSnet Aquila).</li><li>Support system integration activities, helping ensure seamless data flow and interoperability between MES and other enterprise systems (such as ERP, LIMS, automation, and data management platforms) through cross-functional teamwork.</li><li>Analyze manufacturing requirements, collaborate with stakeholders (process engineers, business teams), and translate paper records into digital formats.</li><li>Prioritize and execute support activities to align with project schedules and business needs.</li><li>Author and maintain system and verification documentation, ensuring adherence to GMP, Global, and internal quality standards.</li><li>Demonstrate a high level of integrity and recognize the importance of quality control in pharmaceutical production.</li><li>Perform comprehensive testing of new MES recipes and system changes.</li><li>Troubleshoot MES issues, provide technical support during recipe execution, and resolve incidents in live production.</li><li>Support change management and continuous improvement initiatives contributing to standardization and efficiency.</li><li>Follow Environmental Health and Safety procedures and participate in incident investigations as required.</li><li>Build rapport and communicate effectively with colleagues across and outside the MES team.</li><li>Support business users, ensuring their requirements are understood and delivered at or above expectations.</li><li>The role will evolve to require Off Hours Support for MES systems.</li></ul><br>Qualifications<br><br><ul><li>Bachelor’s degree in Engineering, Computer Science, or related discipline with a minimum of (two) 2 years of relevant experience.</li><li>Experience in MES recipe authoring or supporting IT applications in GMP-regulated manufacturing (pharma, biotech, medical devices).</li><li>Familiarity with MES solutions (POMSnet Aquila, PharmaSuite, Syncade, Werum PAS-X, or similar), and a working understanding of ISA-88/ISA-95 standards.</li><li>Working understanding of manufacturing processes, pharmaceutical/biopharma regulations, and data integrity principles.</li><li>Experience supporting the authoring of requirements, specifications, and validation/verification protocols.</li><li>Ability to manage multiple tasks, support results-driven work, and collaborate effectively across diverse functions.</li><li>Good troubleshooting, communication, documentation, and organizational skills.</li><li>Detail-oriented, proactive, and self-motivated work ethic.</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our short-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. </p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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<p><span><b>International Medical Mission</b></span></p><br><br><span><i>Supportive to our colleagues and trusted partners in the technological transformation of international healthcare ecosystems, we bring pioneering science to patients, through equitable end-to-end impact.</i></span><br><p><span><b>PURPOSE</b></span></p><br><br><p><span>The North Africa Cluster Medical Lead is the single point of medical accountability for Morocco, Algeria, Tunisia and Libya. The role provides leadership to all in-country and cross-cluster medical functions and is the senior medical voice of Pfizer across the cluster, both internally and externally, acting as the Pfizer CMAO representative in the local environment.</span></p><br><br><p><span>The role has both an internal and an external focus. Internally, it shapes and executes the cluster medical strategy, ensures medical readiness for launches, safeguards compliance and medical quality, and builds high-performing teams that use AI and digital tools responsibly. Externally, it strengthens Pfizer’s scientific leadership, builds trusted partnerships across the healthcare ecosystem, and advances patient outcomes through evidence generation and operational excellence.</span></p><br><br><p><span><b>SCOPE</b></span></p><br><br><ul><li><span>Leading medical strategy and execution across a diverse, multi-country cluster with varying healthcare systems, regulatory environments and levels of market maturity</span></li></ul><ul><li><span>Acting as the primary medical partner to country and cluster leadership teams</span></li></ul><ul><li><span>Providing scientific guidance, insights and expertise across the broad Pfizer portfolio and multiple therapeutic areas</span></li></ul><ul><li><span>Role modelling Pfizer’s values and behaviors, and the purpose of breakthroughs that change patients’ lives</span></li></ul><ul><li><span>Driving transformation in medical affairs through innovative, agile and efficient ways of working, including the responsible use of AI, digital and data</span></li></ul><ul><li><span>Building, developing and retaining high-performing medical teams across markets</span></li></ul><ul><li><span>Strengthening Pfizer’s external scientific leadership and credibility in North Africa</span></li></ul><p><span><b>GEOGRAPHIC SCOPE</b></span></p><br><br><p><span>Morocco, Algeria, Tunisia and Libya</span></p><br><br><p><span><b>REPORTING LINE</b></span></p><br><br><p><span>Reports to the VP, </span><span><span>MERA Cluster & ACCORD/GCAP Regional Medical Lead</span></span></p><br><br><p><span><b>RESOURCES MANAGED</b></span></p><br><br><ul><li>Country medical leads across Morocco, Algeria, Tunisia and Libya, reporting to this role directly</li></ul><ul><li><span>Medical affairs teams across the North Africa cluster</span></li></ul><ul><li><span>Medical affairs budgets across the cluster</span></li></ul><p><span><b>ORGANIZATIONAL RELATIONSHIPS</b></span></p><br><br><ul><li><span>Leadership forums: North Africa country and cluster leadership teams; MERA regional medical and leadership forums, as relevant</span></li></ul><ul><li><span>Peer medical leadership: MERA Cluster and Country Medical Leads, and Cluster Medical Leads of other Emerging Markets regions</span></li></ul><ul><li><span>Cross-functional: Commercial, Corporate and Public Affairs, Policy, Regulatory, Access, Patient Advocacy, Worldwide Medical & Safety (WMS), WRD, GPD, global and category medical organizations, People Experience (PX), Legal and Compliance</span></li></ul><ul><li><span>External: key opinion leaders, medical and scientific societies and associations, academic and clinical centers, health authorities and regulators, government and payers (in partnership with the appropriate functions), patient organizations, healthcare entities and systems, NGOs and relevant multilateral and civil society organizations in a compliant manner</span></li></ul><p><span><b>KEY RESPONSIBILITIES</b></span></p><br><br><p><span><b>1. Medical Strategy & Execution</b></span></p><br><br><ul><li><span>Develop and execute the cluster medical vision, strategy and operating plan, aligned with regional and global priorities</span></li></ul><ul><li><span>Directly lead medical affairs, ensuring operational excellence in customer-facing medical activities</span></li></ul><ul><li><span>Lead and partner through every step of go-to-market and launch: country selection, disease awareness, internal readiness, medical outreach, implementation and sustainability</span></li></ul><ul><li><span>Drive prioritization and resource allocation, with a sharp focus on activities that deliver customer and patient impact</span></li></ul><p><span><b>2. Evidence Generation & Scientific Strategy</b></span></p><br><br><ul><li><span>Ensure high-quality evidence generation and data dissemination in partnership with global medical platforms</span></li></ul><ul><li>Ensure quality and integrity of evidence generation, including GCP, ethics approvals, publication and data integrity</li></ul><ul><li><span>Integrate insight generation, HTA readiness and stakeholder engagement into one evidence strategy across launch, in-line and mature products</span></li></ul><ul><li><span>Support healthcare system capability development, medical education and up-to-date portfolio awareness for healthcare professionals</span></li></ul><ul><li><span>Demonstrate the value of the portfolio through country and TA-specific metrics on patient outcomes and healthcare system impact</span></li></ul><ul><li>Feed North Africa insights and unmet-need data into regional and global strategy and the pipeline</li></ul><ul><li><span>Ensure scientific leadership and TA expertise through rigorous training and a single global medical “truth”, asset by asset</span></li></ul><p><span><b>3. External Scientific Leadership & Partnerships</b></span></p><br><br><ul><li><span>Represent Pfizer to KOLs, academic institutions, regulators, government and payers (in partnership with the appropriate functions), and during business development discussions</span></li></ul><ul><li><span>Build and sustain peer-to-peer relationships and external partnerships with medical societies, associations, patient organizations and healthcare systems in a compliant manner</span></li></ul><ul><li><span>Contribute to policy and advocacy engagement in line with Pfizer policy engagement and lobbying policies, and ensure alignment with cross functional advocacy teams</span></li></ul><ul><li><span>Understand and articulate medical care gaps and unmet need in the cluster to shape compliant medical engagements</span></li></ul><p><span><b>4. Medical Communications, Governance, Compliance & Quality</b></span></p><br><br><ul><li><span>Drive medical omnichannel communication on the risks and benefits of Pfizer medicines in a non-promotional, scientifically balanced and fully compliant manner</span></li></ul><ul><li><span>Ensure adherence to applicable laws, regulations, industry codes and Pfizer policies and procedures across all markets in the cluster</span></li></ul><ul><li>Be accountable for audit, inspection and corporate governance readiness, quality events and CAPA completion across the cluster, working with medical quality and governance teams</li></ul><ul><li>Ensure timely and appropriate handling of product quality complaints, medical information inquiries and compliance concerns</li></ul><ul><li>Ensure timely reporting of adverse events, product complaints and special situations by medical teams, in line with pharmacovigilance requirements</li></ul><ul><li>Ensure medical materials and communications receive medical review and approval by qualified personnel</li></ul><ul><li>Ensure SOP and training compliance, and alignment of local procedures with global standards</li></ul><ul><li><span>Provide medical guidance to regulatory, safety and commercial teams in support of key product maintenance</span></li></ul><ul><li><span>Chair or delegate attendance at Cluster Medical Councils to maintain compliance, information flow and timely resolution of issues</span></li></ul><ul><li><span>Maintain and role-model a high standard of integrity and a culture of compliance</span></li></ul><p><span><b>5. Leadership & Talent Development</b></span></p><br><br><ul><li><span>Lead, coach and develop high-performing teams; build leadership bench strength and address performance gaps and build team capability where needed</span></li></ul><ul><li><span>Foster an inclusive culture of innovation, accountability, collaboration and a lightspeed mindset</span></li></ul><ul><li><span>Build change-agile teams and lead colleagues through organizational and external change</span></li></ul><p><span><b>6. Cross-Functional Partnership & Performance</b></span></p><br><br><ul><li><span>Partner with country and cluster leaders and represent all medical and related functions in leadership teams, as the One Medical voice of Pfizer</span></li></ul><ul><li><span>Develop compliant medical plans with clear KPIs; drive medical impact through qualitative and quantitative metrics</span></li></ul><ul><li><span>Optimize medical resources and drive efficiency and synergies with regional and cross-category medical teams</span></li></ul><p><span><b>REQUIRED & PREFERRED EXPERIENCE & QUALIFICATIONS</b></span></p><br><br><p><span><b>Basic Qualifications</b></span></p><br><br><ul><li><span>An MD, Pharm D or equivalent doctoral degree</span></li></ul><ul><li><span>10+ years in medical affairs and/or clinical drug development in the pharmaceutical or biotechnology industry, with in-depth knowledge of multiple therapeutic areas</span></li></ul><ul><li><span>Line management experience of medical teams in a country organization, cluster or headquarters</span></li></ul><ul><li><span>Demonstrated medical leadership at country, cluster, regional or above-country level, including development and execution of medical strategies and plans</span></li></ul><ul><li><span>Demonstrated experience building external medical partnerships with academic institutions, medical societies, patient organizations or healthcare systems in a compliant manner</span></li></ul><ul><li><span>Strong understanding of healthcare systems, regulatory and pharmacovigilance requirements, and industry codes of practice</span></li></ul><ul><li><span>Ability to develop, articulate and communicate complex medical strategies to internal and external stakeholders</span></li></ul><ul><li><span>Fluency in spoken and written English</span></li></ul><p><span><b>Preferred Qualifications</b></span></p><br><br><ul><li><span>Strong command of French is highly preferred, and Arabic is a plus, in spoken and written form</span></li></ul><ul><li><span>Prior Leadership position in North Africa</span></li></ul><ul><li><span>Board certification or license in a relevant medical discipline; additional advanced clinical or scientific degree</span></li></ul><ul><li><span>Strong business acumen, including budget management and financial impact forecasting</span></li></ul><ul><li><span>Ability to achieve results through influence in a matrix organization, with strong internal and external alliance building</span></li></ul><ul><li><span>Active engagement with pharmaceutical associations and patient groups; teaching or academic appointments are a plus</span></li></ul><ul><li><span>Track record of change leadership, with sound decision-making under uncertainty</span></li></ul><p><span><b>CRITICAL CAPABILITIES</b></span></p><br><br><ul><li><span>Scientific Credibility: owns scientific credibility across markets of different size and complexity, balancing rigor and the non-promotional boundary with commercial and patient urgency</span></li></ul><ul><li><span>Evidence & Scientific Strategy: Designs and executes differentiated evidence strategies that deliver patient impact across the lifecycle</span></li></ul><ul><li><span>Shaping the Future: Anticipates what is next, influences upstream decisions and translates future scenarios into strategic choices today</span></li></ul><ul><li><span>Business Transformation: Leads change, simplifies ways of working and applies AI, digital and data fluently and responsibly</span></li></ul><ul><li><span>External Acumen: Navigates and influences the external environment, treating patient access as a critical strategic capability</span></li></ul><ul><li><span>Enterprise Leadership: Leads with an enterprise-first mindset, builds a culture of inclusion, trust and accountability, and develops talent</span></li></ul><ul><li>Integrity & Quality Mindset: Role-models integrity, owns compliance and medical quality, and builds a culture of speaking up and continuous improvement</li></ul><p><span><b>TRAVEL & WORK REQUIREMENTS</b></span></p><br><br><ul><li><span>Regular travel across the North Africa cluster to lead geographically distributed teams and engage external stakeholders in person</span></li></ul><ul><li><span>Regular participation in meetings across multiple time zones, including occasional meetings outside standard local business hours</span></li></ul><br><p>Please note that relocation package would be considered and supported according to the final talent selection.</p><br><br><br><p><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><br><br><br><br><p>To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on <span><u>Pfizer Careers</u></span>.</p><br><br><br><br>Medical<br><br><br> </div>
<p><br></p> <p> <b>Purpose: </b>The Medical Science Liaison (MSL) is a field-based scientific expert responsible for cultivating strategic peer-to-peer partnerships with Key Opinion Leaders (KOLs) and leading specialists. The role acts as a scientific bridge between Johnson & Johnson Innovative Medicine and the external medical community, driving evidence-based clinical understanding, non-promotional scientific exchange, and the execution of country- or therapy-specific Medical Affairs strategies.</p> <br> <p> <b>You will be responsible for:</b> </p> <ul> <li> <b>To keep abreast of medical and scientific knowledge.</b> <ul> <li>Continuously update their knowledge of products, patient s treatment trends and clinical activities and studies conducted within the therapeutic area in their region.</li> </ul> </li> <li> <b>Development and maintenance of a contact network with Leading Specialists.</b> <ul> <li>Understands their needs, key value drivers, practical treatment patterns and scientific activities within the therapeutic area</li> <li>Communicates value of company products, incl. formulary discussions</li> <li>Through scientific interactions, champions medical benefits of products and contribute to fostering innovative approaches</li> <li>Represents the company within therapeutic area professional associations in cooperation with Medical Advisor/ Medical Lead/Medical Director</li> </ul> </li> <li> <b>Proactive and reactive communication of medical scientific data to Leading Specialists and broader external health-care-related audiences:</b> <ul> <li>Communicates directly and proactively scientific information of our products within the approved label</li> <li>Communicates non-promotional general information about our company, including description of research and development programs</li> <li>Responds to unsolicited scientific queries of customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents</li> </ul> </li> <li> <b>Organization and participation in Medical Education activities:</b> <ul> <li>Identify/support/educate speakers</li> <li>Build Medical Education programs with scientific third parties</li> </ul> </li> <li> <b>Organization and participation in Advisory Boards in cooperation with Medical Advisor/Medical Lead/Medical Director</b> </li> <li> <b>Provision of scientific support to company Sales Representative</b> <ul> <li> Provides medical and product training and scientific support to Sales Representatives in coordination with the Training Department as appropriate</li> <li> Acts as a reference point to Sales Representatives for any scientific query, in collaboration with Medical Information as appropriate</li> </ul> </li> <li> <b>Support Medical Affairs study execution</b> <ul> <li>Supports the set up and follow up of registries and other non-interventional Medical Affairs studies</li> <li>Propose investigators and sites for interventional and non-interventional Medical Affairs studies</li> <li>Participate in investigator meetings preparation, recruitment follow-up and study result presentation</li> <li>Receives investigator proposals for IIS and to ensure they are discussed within the Medical Affairs department for decision</li> </ul> </li> <li> <b>Through scientific interactions, gain valuable insight into treatment patterns, and scientific activities in the therapeutic area and provide input to the company Medical Affairs Plan / business decision-making</b> </li> </ul> <p> <br> <b>Qualifications / Requirements:</b> </p> <ul> <li>Doctorate in pharmacy or advanced healthcare sciences </li> <li>Minimum of 3 years of relevant experience in a multinational pharmaceutical company is an advantage</li> <li>Experience in Oncology therapy area is an advantage</li> <li>Scientific acumen and communication skills in order to be accepted by Leading Specialists in peer- to-peer relationship</li> <li>Highly customer focused with an awareness of the importance of business results</li> <li>Innovative with the ability to coordinate and drive a complex and changing environment </li> </ul> <br><p><strong>Desired Candidate Profile</strong></p><ul><li>Doctorate in pharmacy or advanced healthcare sciences </li><li>Minimum of 3 years of relevant experience in a multinational pharmaceutical company is an advantage</li><li>Experience in Oncology therapy area is an advantage</li><li>Scientific acumen and communication skills in order to be accepted by Leading Specialists in peer- to-peer relationship</li><li>Highly customer focused with an awareness of the importance of business results</li><li>Innovative with the ability to coordinate and drive a complex and changing environment </li></ul>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution<br>of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill<br>strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in<br>alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or<br>Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and<br>personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial<br>oversight to staff members, including performance assessment, training and feedback, resolution of personnel<br>issues, and management of talent retention.</p><br><p><br>Responsibilities :</p><br><ul><li>This role will report to the Director of Pub Execution to lead a team of publication managers. This role will lead, support, and develop a team by setting clear expectations, communicating priorities, and providing regular coaching and feedback. Hire and onboard employees as needed; support performance and career development; recognize contributions; and address performance or workplace concerns promptly and fairly. Foster an inclusive, respectful, and collaborative environment, and follow applicable company policies and people practices.</li><li>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</li><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul><br>Qualifications<br><br><ul><li>Minimum of Bachelor’s Degree required. PhD, PharmD, Master’s Degree preferred. Relevant professional certification/credential (eg, CMPP, AMWA) is a plus.</li><li>4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg, medical communication agency) experience required</li><li>Demonstrated abilities in a leadership capacity required</li><li>Ability to understand and interpret medical data require</li><li>Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required</li><li>Knowledge of clinical/scientific publication structure, content, and quality. Knowledge of scientific publication regulations and best practices</li><li>Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences</li><li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record</li><li>Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise</li><li>Microsoft Office and Internet navigation proficiencies essential</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our long-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution<br>of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill<br>strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in<br>alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or<br>Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and<br>personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial<br>oversight to staff members, including performance assessment, training and feedback, resolution of personnel<br>issues, and management of talent retention.</p><br><p><br>Responsibilities :</p><br><ul><li>This role will report to the Director of Pub Execution to lead a team of publication managers. This role will lead, support, and develop a team by setting clear expectations, communicating priorities, and providing regular coaching and feedback. Hire and onboard employees as needed; support performance and career development; recognize contributions; and address performance or workplace concerns promptly and fairly. Foster an inclusive, respectful, and collaborative environment, and follow applicable company policies and people practices.</li><li>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</li><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul><br>Qualifications<br><br><ul><li>Minimum of Bachelor’s Degree required. PhD, PharmD, Master’s Degree preferred. Relevant professional certification/credential (eg, CMPP, AMWA) is a plus.</li><li>4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg, medical communication agency) experience required</li><li>Demonstrated abilities in a leadership capacity required</li><li>Ability to understand and interpret medical data require</li><li>Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required</li><li>Knowledge of clinical/scientific publication structure, content, and quality. Knowledge of scientific publication regulations and best practices</li><li>Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences</li><li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record</li><li>Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise</li><li>Microsoft Office and Internet navigation proficiencies essential</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</li><li>This job is eligible to participate in our long-term incentive programs. </li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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Job : <p>Assigned to the Health Center of Lydex Rabat, the sports doctor plays a central role in the monitoring, prevention, and medical care of student athletes. In collaboration with the medical team and sports staff, they ensure the health, safety, and well-being of the athletes while contributing to the optimization of their performance.</p><br><br><ul><li>Ensure regular medical monitoring of student athletes, checking their general health status and their fitness for training and competition.</li><li>Conduct medical assessments, fitness tests, and functional evaluations necessary for candidate athletes as part of the admission process to Lydex.</li><li>Inform and educate athletes, coaches, and staff about issues related to doping, its health risks, and anti-doping regulations.</li><li>Monitor the adaptation of training loads in conjunction with coaches and physical trainers, to ensure the safety and well-being of athletes, while strictly respecting medical confidentiality.</li><li>Provide medical care by administering necessary treatments when the athletes' clinical situation requires it.</li><li>Implement prevention and health education actions for athletes, coaches, and the technical team (nutrition, sleep, stress management, overtraining, etc.).</li><li>Organize and lead awareness sessions on topics relevant to high-level athletes (injury prevention, lifestyle, mental health, recovery, etc.).</li><li>Coordinate medical care with physiotherapists, physical trainers, and external specialists, and approve medical decisions related to rehabilitation or return-to-sport protocols.</li><li>Participate in the management of medical emergencies, provide first aid, and refer athletes to specialized facilities when necessary.</li><li>Ensure the updating of internal medical protocols and their application by the entire medical and paramedical team.</li><li>Maintain scientific and regulatory knowledge to integrate best practices in sports medicine, prevention, and performance.</li></ul> <br> <br> Required profile : AREAS OF EXPERTISEKNOWLEDGE / TECHNICAL SKILLS / DIPLOMAS / CERTIFICATES<ul><li>Doctor of Medicine with a specialization or further training in sports medicine.</li><li>Previous experience in sports medicine.</li><li>Good knowledge of sports training biology.</li><li>Strict adherence to medical confidentiality.</li></ul>SKILLS<ul><li>Conduct medical examinations and health assessments for athletes.</li><li>Diagnose and manage sports-related injuries.</li><li>Provide medical follow-up for athletes and injury prevention.</li><li>Collaborate with the medical team and sports staff.</li></ul>PERSONAL ATTRIBUTES<ul><li>Good listening skills</li><li>Team spirit</li><li>Rigor and professionalism</li><li>Responsiveness</li><li>Sense of responsibility</li><li>Discretion and respect for medical confidentiality.</li></ul> <br><br> </div>
<h2 class="h5">Job description</h2>
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<br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><br><br>Job Description<br><br><p>The Field Medical Director is the regional Field Medical Leader responsible for leading, coaching, and developing Field Medical teams to deliver high-quality, compliant scientific engagement and identify impactful healthcare professional perspectives and Scientific Intelligence. The role translates medical and therapeutic area strategy into regional field execution, elevates the quality and consistency of scientific exchange, and ensures that field-captured insights inform medical planning and evidence strategy. Through strong people leadership and scientific stewardship, the Field Medical Director strengthens AbbVie’s field medical impact across the region. </p><br><p>Responsibilities: </p><br><ul><li><p>Lead, coach, and develop Field Medical Team members to deliver consistent, high-quality, non-promotional scientific engagement for the multiple myeloma therapeutic area. </p><br></li></ul><ul><li><p>Translate medical and therapeutic area strategy into clear regional field priorities and execution plans. </p><br></li></ul><ul><li><p>Establish expectations and standards for scientific exchange, healthcare professional perspectives and Scientific Intelligence, and compliant field execution. </p><br></li></ul><ul><li><p>Review, interpret, and elevate field-identified healthcare professional perspectives and Scientific Intelligence to inform medical planning and evidence needs. </p><br></li></ul><ul><li><p>Provide ongoing coaching and feedback to strengthen scientific capability, judgment, and communication skills across the Field Medical Team. </p><br></li></ul><ul><li><p>Partner with Medical Affairs and Health Impact (MHI) leadership to align regional execution with medical objectives and evidence strategies. </p><br></li></ul><ul><li><p>Collaborate with cross-functional partners through the In-Field Team (IFT) to support aligned regional engagement. </p><br></li></ul><ul><li><p>Monitor regional field activity, healthcare professional perspectives and Scientific Intelligence quality, and performance trends to identify opportunities for improvement. </p><br></li></ul><ul><li><p>Support talent development, onboarding, and succession planning within the Field Medical Organization, including conducting regular field ride observations with all direct report MSLs. </p><br></li></ul><p>Territory includes: New England, PA, OH, IN, MI</p><br><br>Qualifications<br><br><ul><li><p>Open to remote candidates in the territory near an international airport. This is the first in a planned series of postings for this team. </p><br></li></ul><ul><li><p>Advanced scientific degree required (PharmD, PhD, MD, or equivalent experience). </p><br></li></ul><ul><li><p>Strong understanding of multiple myeloma disease area, clinical evidence, and the role of Field Medical within Medical Affairs. </p><br></li></ul><ul><li><p>Experience in Field Medical, Medical Affairs, scientific or healthcare roles within the pharmaceutical or life sciences industry. </p><br></li></ul><ul><li><p>Demonstrated experience leading, coaching, and developing field-based scientific professionals. </p><br></li></ul><ul><li><p>Experience successfully translating medical strategy into field execution and performance expectations. </p><br></li></ul><ul><li><p>Experience interpreting and leveraging field-identified insights to inform medical or evidence planning. </p><br></li></ul><ul><li><p>Experience collaborating effectively with cross-functional partners within Medical Affairs and the In-Field Team (IFT). </p><br><p><strong>Competencies </strong></p><br></li><li><p>Leads Field Medical Teams by applying strong scientific knowledge and sound judgment to guide high-quality scientific engagement. </p><br></li><li><p>Coaches and develops scientific capability by providing clear direction, feedback, and role modeling of scientific excellence. </p><br></li><li><p>Translates medical and therapeutic area strategy into actionable regional priorities and execution standards. </p><br></li><li><p>Uses field healthcare professional perspectives, Scientific Intelligence and performance data to inform decision making and continuous improvement of field execution. </p><br></li><li><p>Builds an environment of accountability, trust, and collaboration that supports consistent, compliant scientific engagement. </p><br></li><li><p>Applies strong people leadership skills to motivate, engage, and retain high-performing field medical talent. </p><br></li><li><p>Collaborates with Medical Affairs and Health Impact (MHI) leaders and cross-functional partners to align regional field activity with broader medical objectives. </p><br></li><li><p>Communicates clearly and effectively to connect strategy, expectations, and performance outcomes for Field Medical Teams. </p><br><p><strong>Key Stakeholders</strong></p><br></li><li><p>Field Medical Leadership and Field Medical team members </p><br></li><li><p>Healthcare professionals, scientific stakeholders, and regional healthcare decision makers engaged by MSL and MOSL teams </p><br></li><li><p>MHI and therapeutic area medical leadership </p><br></li><li><p>In-field cross-functional teams </p><br></li><li><p>Health Economics and Outcomes Research (HEOR) partners </p><br></li><li><p>Evidence Generation and Clinical Research partners </p><br></li><li><p>Market Access and Value Strategy colleagues </p><br></li><li><p>Regulatory, safety, and medical information colleagues </p><br></li><li><p>Learning and development partners supporting field medical capability </p><br></li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: </p><br><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. </p><br></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.</p><br></li><li><p>This job is eligible to participate in our long-term incentive programs. </p><br></li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. </p><br><p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>
<h2 class="h5">Job description</h2>
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<br> Company culture : <p><strong>Akdital </strong>is driven by a strong <strong>performance-oriented</strong> culture, where ambition, high standards, and continuous improvement are key to delivering exceptional healthcare.<br>
This competitive mindset is balanced by a real commitment to <strong>innovation</strong>, supporting the development of new medical and organizational practices.<br>
<strong>Collaboration</strong> also plays an important role, with solid teamwork and supportive management in a demanding environment.<br>
A structured and disciplined approach ensures the <strong>quality, safety, and reliability</strong> essential to the medical sector.
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<br> Job : <p>Join a dynamic player in the <strong>healthcare</strong> sector located in <strong>Dakhla</strong>. As an <strong>accounting assistant</strong>, integration into a dedicated team allows you to actively contribute to financial rigor and the daily management of economic flows essential for the smooth operation of health services.</p><br><br><p>The main goal is to ensure fluid and precise accounting management by actively participating in the processing of current financial operations. The rigorous maintenance of records and the support provided to the accounting function aim to guarantee data reliability and compliance with legal obligations inherent to the healthcare field.</p><br><br><p>On a daily basis, the tasks involve administrative and accounting management:</p><br><br><ul><li>Entry of accounting entries and supporting documents.</li><li>Monitoring of supplier and customer invoices with particular attention to account clearing.</li><li>Active participation in bank reconciliations.</li><li>Preparation of regular tax declarations.</li><li>Secure filing and archiving of financial documents to ensure exemplary traceability.</li></ul> <br> Required profile : <p>Higher education of <strong>bac +2</strong> level in <strong>management, accounting, or finance</strong> is essential to master the technical fundamentals of the role.</p><br><br><p>Successful professional experience of <strong>1 to 3 years</strong> in a similar role is required to demonstrate an immediate ability to handle accounting flows.</p><br><br><p>Rigor and organizational skills are at the core of the expectations for this position. The skills sought include:</p><br><br><ul><li>Proficiency in computer tools and accounting software.</li><li>Solid understanding of fundamental accounting principles.</li><li>Analytical skills and attention to detail.</li><li>Collaborative spirit essential for working within a multidisciplinary team.</li></ul><p>If this profile matches the expectations and professional ambition, it is time to apply now by clicking on "Send my CV to the recruiter".</p><br><br> <br><br> </div>
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Job : <p>As part of the development of its team in Casablanca, Mira Clinic is recruiting Medical Advisors / Sales Consultants in tele-selling to join its team specializing in medical tourism.</p><br><br><p><strong>Your missions</strong></p><br><br><ul><li>Contact clients interested in our medical services.</li><li>Identify their needs and provide them with suitable information and solutions.</li><li>Ensure professional and regular follow-up with prospects.</li><li>Coordinate with the medical team to obtain treatment plans.</li><li>Accompany the client from the first contact until the confirmation of their booking.</li><li>Achieve sales targets while ensuring an excellent customer experience.</li></ul><p><strong>What we offer you</strong></p><br><br><ul><li>A fixed salary of 5,000 MAD, supplemented by an attractive commission of up to 2% of the turnover generated.</li><li>A commission system that allows the best profiles to significantly increase their income based on their results.</li><li>Comprehensive professional training on our medical services, patient counseling, and sales techniques.</li><li>Real opportunities for advancement and promotion in medical tourism and sales.</li><li>A professional work environment that values performance, commitment, and results.</li></ul><p><strong>Working conditions</strong></p><br><br><p>Full-time, on-site position in Casablanca: 5 days a week, 8 hours a day. Two fixed days off: Sunday and Monday.</p><br><br> <br> Required profile : <p>We are looking for profiles with real experience in telephone sales, capable of building trust and turning prospect requests into confirmed bookings.</p><br><br><ul><li>Excellent command of French, both spoken and written - an essential requirement.</li><li>Perfect command of Moroccan Darija.</li><li>Previous experience in tele-selling / Telesales.</li><li>Experience in medical tourism or the medical sector is a real asset.</li><li>Excellent communication, persuasion, and negotiation skills.</li><li>Ability to handle objections and close sales.</li><li>Sense of follow-up, organization, and customer relations.</li><li>Professional, dynamic, ambitious profile, focused on results and objectives.</li></ul> <br><br> </div>
<h2 class="h5">Job description</h2>
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Job : <p>As part of the development of its team in Casablanca, Mira Clinic is recruiting Medical Advisors / Sales Advisors - Telesales to join its team specialized in medical tourism.</p><br><br><p><strong>Your missions</strong></p><br><br><ul><li>Contact clients interested in our medical services.</li><li>Identify their needs and provide them with suitable information and solutions.</li><li>Ensure professional and regular follow-up with prospects.</li><li>Coordinate with the medical team to obtain treatment plans.</li><li>Accompany the client from the first contact until the confirmation of their booking.</li><li>Achieve sales objectives while ensuring an excellent customer experience.</li></ul><p><strong>What we offer you</strong></p><br><br><ul><li>A fixed salary of 5,000 MAD, supplemented by an attractive commission of up to 2% of the turnover achieved.</li><li>A commission system allowing the best profiles to significantly increase their income based on their results.</li><li>Comprehensive professional training on our medical services, patient counseling, and sales techniques.</li><li>Real opportunities for growth and promotion in medical tourism and sales.</li><li>A professional work environment that values performance, commitment, and results.</li></ul><p><strong>Working Conditions</strong></p><br><br><p>Full-time, on-site position in Casablanca: 5 days a week, 8 hours a day. Two fixed days off: Sunday and Monday.</p><br><br> <br> <br> Required profile : <p>We are looking for profiles with real experience in telephone sales, capable of building trust and turning prospect requests into confirmed bookings.</p><br><br><ul><li>Excellent command of French, both spoken and written - an essential requirement.</li><li>Perfect command of Moroccan Darija.</li><li>Previous experience in telesales.</li><li>Experience in medical tourism or the medical sector is a real asset.</li><li>Excellent communication, persuasion, and negotiation skills.</li><li>Ability to handle objections and close sales.</li><li>Sense of follow-up, organization, and customer relations.</li><li>Professional, dynamic, ambitious profile, focused on results and objectives.</li></ul> <br><br> </div>
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