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associate director medical affairs egypt

Organon Pharmaceuticals

<div>Job Title: Assoc. Dir, Medical Affairs
Location / Site: Cairo
The Position
The Medical Advisor holds primary responsibility within the country for the development and execution of the Medical Affairs Plans in his/her therapeutic areas under the guidance and supervision of the META Cluster Medical Lead. Additionally, the Medical Advisor provides Medical Affairs therapeutic area support through engaging with Scientific Leaders (SLs) / Key Decision Makers (KDMs), driving scientific initiatives and supporting the field force. 
Responsibilities
Scientific and Technical Leadership<ul><li>Communicate scientific therapy needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels.</li><li>Build trust with the external scientific community via peer-to-peer scientific exchange, research and educational collaborations, interactions with scientific societies and health organizations, publications, etc.</li><li>Provide therapeutic/functional training to assigned teams and affiliate functions.</li><li>Develop and help execute country medical educational programs and symposia.</li><li>Lead country Advisory Boards and Expert Input Forums in line with strategy.</li><li>Participate in and contribute significantly to professional organizations, academic or regulatory working teams.</li><li>Provide scientific inputs for digital initiatives.</li></ul>
Medical Strategy and Therapy Leadership<ul><li>Translate Global Medical Strategies into research, data analysis, scientific communication, educational, and other tactics and solutions that improve patient outcomes and enhance access in the country.</li><li>Ensure effective communication and collaboration between field and Medical through providing scientific and medical support to the Commercial team.</li><li>Evaluate accuracy of promotional materials.</li><li>Provide Medical Affairs therapeutic area support through engaging with SLs/KDMs, driving scientific initiatives and supporting the field force.</li><li>Collect, analyze, and communicate actionable insights at the country level.</li><li>Provide scientific inputs for digital initiatives.</li><li>Successfully collaborate, provide scientific inputs, and lead resolution of Regulatory queries/issues.</li><li>Support execution of and quickly adapt tactical plans to business realities in country.</li><li>Act with ethics and integrity; Provide non-promotional, balanced, reliable and scientific information.</li><li>Support with therapy training content for Sales team.</li><li>Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence.</li><li>Support creation of Medical Affairs Plans along with the TA and META cluster Medical Leads.</li></ul>
Medical Information<ul><li>Provide prompt medical information support, such as research and answering of medical inquiries from external and internal customers.</li></ul>
Required Education, Experience and Skills 
<ul><li>Minimum of 4 year's experience in filed medical affairs.</li><li>
Pharma industry experience required, minimum 5 years in multinational company.</li><li>
Medical degree, PhD, Pharm D or other relevant life sciences degree.</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc.)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Ability to analyze medical literature in order to evaluate the different tendencies in research</li><li>
Strong scientific baseline knowledge in assigned therapeutic area(s).</li><li>
Scientific leadership</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence</li><li>
Strategic planning</li><li>
High level of scientific and ethical integrity.</li><li>
Excellent communication skills, including listening and probing skills, across a variety of internal and external audiences.</li><li>
Strong collaboration and negotiation skills and ability to function within a team environment.</li><li>
Problem solving</li><li>
Analytical skills</li><li>
Understanding of core systems, tools and metrics related to medical literature</li><li>
Excellent written and oral proficiency in English</li><li>
Complex projects management</li><li>
Candidate must be based in Cairo</li></ul>
Secondary Job Description
Who We Are:
Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women&rsquo;s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.
As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.
Search Firm Representatives Please Read Carefully 
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Annualized Salary Range
Annualized Salary Range (Global)
Annualized Salary Range (Canada)
Please Note: Pay ranges are specific to local market and therefore vary from country to country.
Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites
Flexible Work Arrangements:
Shift:
Valid Driving License:
Hazardous Material(s):
Number of Openings:
1 
Requisition ID:R539260</div>

Associate Director, Medical Affairs - Egypt

Merck KGaA

<div>Work Your Magic with us! 
Ready to explore, break barriers, and discover more? We know you&rsquo;ve got big plans &ndash; so do we! Our colleagues across the globe love innovating with science and technology to enrich people&rsquo;s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. 
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. 
Your Role:
Are you passionate about patient safety and looking to make a significant impact in the field of pharmacovigilance? An exciting opportunity has opened up with our company. We are looking to hire a Patient Safety Center Associate and Local Safety Responsible (LSR) for Egypt based locally in the country for the Patient Safety Center Africa.
Responsibilities:<ul><li>
All Pharmacovigilance (PV) related tasks in Egypt where this role will be nominated as local Safety Responsible (LSR) to Egypt Health Authority.
</li><li>Collaborate with a team handling PV activity across other African countries. This is a unique opportunity to work cross-functionally at both local and global levels, driving initiatives that enhance patient safety.</li><li>
As a Patient Safety Center Associate, you will be an integral part of our regional organization, the Patient Safety Center Africa and will be responsible to ensure that individual case safety reports from the local market are appropriately processed and followed up.
</li><li>This role will be responsible for the establishment and maintenance of the marketing authorization holder &lsquo;s pharmacovigilance system while maintaining promoting and improving compliance with local regulatory requirements.</li><li>
Maintain the local PV documentation of the PV systems and perform PV training as applicable. You will contribute to local audits and inspections and will support the preparation of local Risk Management Plan and submission of local aggregate safety report where applicable.
</li><li>Monitor the local PV regulation and properly follow up on the generated activities.</li><li>
Uploading new information, updating records, necessary registrations and submissions to regulators systems with good understanding of Safety Databases.</li><li>
Implementation of PV agreements and perform the required PV activities related to Patient Data collection systems and Clinical studies.</li><li>
Collaborate closely with the Global Organizations as well as the cross-functional teams (local Management, QA, Medical Affairs, Regulatory Affairs Business Unit)</li></ul>
Who you are:
<ul><li>Bachelor Degree of Pharmacy or Medicine.</li><li>
Fluent in written and spoken local language and English.</li><li>
4/5 years in PV or in the pharma industry. Health authority experience is an advantage.</li><li>
Understand business needs, think strategically, and develop risk mitigation strategies.</li><li>
High level of dedication and a strong willingness to perform.</li><li>
You are curious, obsessed with customers and patients and act as the owner to make the right decision while keeping in mind the Company&rsquo;s best interests.</li></ul> 
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! 
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</div>

Patient Safety Center Associate Manager

Merck Healthcare

<div>
 Work Your Magic with us!
 
 
 Ready to explore, break barriers, and discover more? We know you&rsquo;ve got big plans &ndash; so do we! Our colleagues across the globe love innovating with science and technology to enrich people&rsquo;s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
 
 
 United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
 
 
 
 Your Role
 
 
 
 Are you passionate about patient safety and looking to make a significant impact in the field of pharmacovigilance? An exciting opportunity has opened up with our company. We are looking to hire a Patient Safety Center Associate and Local Safety Responsible (LSR) for Egypt based locally in the country for the Patient Safety Center Africa.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 All Pharmacovigilance (PV) related tasks in Egypt where this role will be nominated as local Safety Responsible (LSR) to Egypt Health Authority.
 </li>
 <li>
 Collaborate with a team handling PV activity across other African countries. This is a unique opportunity to work cross-functionally at both local and global levels, driving initiatives that enhance patient safety.
 </li>
 <li>
 As a Patient Safety Center Associate, you will be an integral part of our regional organization, the Patient Safety Center Africa and will be responsible to ensure that individual case safety reports from the local market are appropriately processed and followed up.
 </li>
 <li>
 This role will be responsible for the establishment and maintenance of the marketing authorization holder &lsquo;s pharmacovigilance system while maintaining promoting and improving compliance with local regulatory requirements.
 </li>
 <li>
 Maintain the local PV documentation of the PV systems and perform PV training as applicable. You will contribute to local audits and inspections and will support the preparation of local Risk Management Plan and submission of local aggregate safety report where applicable.
 </li>
 <li>
 Monitor the local PV regulation and properly follow up on the generated activities.
 </li>
 <li>
 Uploading new information, updating records, necessary registrations and submissions to regulators systems with good understanding of Safety Databases.
 </li>
 <li>
 Implementation of PV agreements and perform the required PV activities related to Patient Data collection systems and Clinical studies.
 </li>
 <li>
 Collaborate closely with the Global Organizations as well as the cross-functional teams (local Management, QA, Medical Affairs, Regulatory Affairs Business Unit)
 
 
 </li>
 </ul>
 
 Who You Are
 
 
 
 <ul>
 <li>
 Bachelor Degree of Pharmacy or Medicine.
 </li>
 <li>
 Fluent in written and spoken local language and English.
 </li>
 <li>
 4/5 years in PV or in the pharma industry. Health authority experience is an advantage.
 </li>
 <li>
 Understand business needs, think strategically, and develop risk mitigation strategies.
 </li>
 <li>
 High level of dedication and a strong willingness to perform.
 </li>
 <li>
 You are curious, obsessed with customers and patients and act as the owner to make the right decision while keeping in mind the Company&rsquo;s best interests.
 
 
 </li>
 </ul>
 
 What we offer:
 
 We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
 
 Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
</div>

Giza Systems EG

<div>Giza Systems Cairo, Egypt Posted 18 days ago Unlimited Ref: JB5441190</div>
 <div><div><h4 class="jobSectionHeader">Job Description</h4>
<div><ul><li>As a Corporate Affairs Expert, you will be responsible for overseeing legal matters and market management within a growing environment. Your role will involve handling litigation, providing legal opinions and advice, as well as reviewing and drafting contracts to ensure legal compliance and protection.</li>
<li>Manage all aspects of corporate legal affairs, including litigation, contracts, and legal opinions.</li>
<li>Provide expert legal advice to the organization on a wide range of legal matters.</li>
<li>Review and draft various contracts, agreements, and legal documents.</li>
<li>Monitor and ensure compliance with relevant laws and regulations.</li>
<li>Collaborate with internal teams to address legal issues and mitigate potential risks.</li>
<li>Stay updated on the latest legal developments and industry trends that may impact the organization.</li>
<li>Strong organizational and multitasking skills, with the ability to prioritize tasks and meet deadlines</li>
</ul></div>
<h4 class="jobSectionHeader">Personal Skills</h4>
<div><ul><li>Excellent communication and interpersonal skills.</li>
<li>Attention to detail and problem-solving abilities.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Excellent time management skills and ability to multi-task and prioritize work</li>
<li>Strong organizational and planning skills</li>
<li>Excellent communication and interpersonal skills.</li>
<li>Excellent analytical &amp; problem-solving skills.</li>
<li>Excellent command of verbal and written Frensh &amp; English.</li></ul></div> 

<h4 class="jobSectionHeader">Technical Skills</h4> 
<div><div> 
Bachelor&rsquo;s degree in law or related field.
 
<ul><li>Master's degree is a plus.
</li><li>3 to 5 years of experience
</li></ul>Proven experience working in corporate legal affairs, preferably in a growing market environment.
 
Strong knowledge of corporate law, litigation, contract management, and legal risk assessment.
 
Excellent communication and interpersonal skills.
 
Ability to work well under pressure and manage multiple tasks simultaneously.
 
Detail-oriented with a focus on accuracy and quality in legal work. 
 
</div></div><h4 class="jobSectionHeader">Education</h4>
<div>Bachelor&rsquo;s degree in Law</div> 
</div><div></div><div><div><h4 class="jobSectionHeader">Job Details</h4>
<div>Job Location Cairo, Egypt
</div><div>Company Industry System Integrator
</div><div>Company Type Employer (Private Sector)
</div><div>Job Role Legal
</div><div>Employment Type Employee
</div><div>Job Division CPCSO
</div></div><div><h4 class="jobSectionHeader">Preferred Candidate</h4>
<div>Career Level Mid Career
</div><div>Years of Experience Min: 3 Max: 5
</div><div>Degree Bachelor's degree</div></div></div></div>
 <div></div><div><div><div><h3 class="jobSectionHeader">Giza Systems</h3>
<div>Integration Cairo, Egypt http://www.gizasystems.com
</div></div></div>Giza Systems, a leading systems integrator in the MEA region, designs and deploys industry-specific technology solutions for asset-intensive industries such as the Telecoms, Utilities, Oil &amp; Gas, Transportation and other market sectors. We help our clients streamline their operations and businesses through our portfolio of solutions, managed services, and consultancy practice. Our te... am of 1000 professionals are spread throughout the region with anchor offices in Cairo, Riyadh, Dubai, Doha, Nairobi, Dar-es-Salaam, Abuja, Kampala and New Jersey, allowing us to service an ever-increasing client base in over 40 countries.</div>

Corporate Affairs Expert

AstraZeneca

<div>Job Title: Nominated Signatory &amp; Medical Excellence Lead
Introduction to role:
Are you ready to uphold the highest standards of medical governance while accelerating field excellence to deliver better outcomes for patients? This role places you at the center of ethical decision-making and capability building, ensuring that every activity, material, and interaction reflects our standards and enables impact at pace.
You will bridge rigorous compliance with practical execution, helping teams move fast and do the right thing. Can you translate strategy into measurable improvements that raise the quality and reach of medical engagement? Join us to combine science, ethics, and operational excellence in a dynamic environment where bold ideas and disciplined delivery go hand in hand.
Accountabilities:<ul><li>
Ethical Interactions Governance: Own and maintain local Ethical Interactions (EI) SOPs; translate global Code of Conduct into robust local procedures covering patient interactions, digital communications, diagnostics, patient affordability, and external funding.</li><li>
Nominated Signatory Leadership: Lead a team of risk assurance managers/signatories; review and approve materials and activities to meet ABAC, data privacy, local regulatory, and company standards; sign HCP/HCO agreements on behalf of the business.</li><li>
External Funding Oversight: Chair the Ethical Interactions Committee; assess, approve, and monitor external funding and third‑party engagements, ensuring transparency, fairness, and appropriate documentation.</li><li>
Risk and Assurance: Conduct first-line monitoring and quality checks; partner with Compliance and Assurance to execute risk assessments, define CAPAs, and track remediation to closure with evidence and sustainability plans.</li><li>
Medical Quality and Standards: Guide medical and marketing collaboration to ensure scientific accuracy, fair balance, and adherence to codes and SOPs across congresses, advisory boards, digital engagement, and field medical activities.</li><li>
Digital Compliance: Govern compliant HCP digital engagement platforms and content, ensuring consent, privacy-by-design, and appropriate content governance across channels.</li><li>
Process Improvement: Drive simplification and continuous improvement of governance processes, templates, and systems; embed controls proportionate to risk while enabling business agility.</li><li>
Cross-Functional Partnership: Advise cross‑functional teams on ethical and governance considerations for complex initiatives, mega events, and interactions with government officials.</li><li>
Medical Excellence: Purpose Elevate Medical Affairs capability across Egypt by defining competency standards, driving robust onboarding and continuous development for Medical Science Liaisons (MSLs) and Medical Advisors, and owning certification and quality assurance to improve scientific engagement, evidence generation readiness, and cross-functional impact.</li><li>
Liaise with the Global &amp; International Medical Excellence Team in connection to excellence programs, localize relevant initiatives to Egypt market as aligned with local strategy and compliance, and seek out opportunities for cross-market collaboration.</li><li>
Improve scientific engagement quality, call planning, narratives, objection handling, compliant interactions, and insight capture/translation.</li><li>
Equip medical managers with coaching requirements as per AZ standards.</li></ul>
Essential Skills/Experience:<ul><li>
Education: Bachelor&rsquo;s degree in pharmacy or related life sciences field required.</li><li>
Experience: 7+ years in Medical Affairs/Compliance/Governance within pharma, including direct Nominated Signatory or equivalent approval authority.</li><li>
Expertise: Strong knowledge of ABAC, Data Privacy, EI codes, GxP fundamentals, and Egypt regulatory frameworks; audit and CAPA lifecycle management; digital engagement governance.</li><li>
Risk assessment, SOP authorship, stakeholder management, training design/delivery, analytical problem solving, change management, and clear written/oral communication in English</li></ul>
 Desirable Skills/ Experience:<ul><li>
Certifications : GCP/GVP quality, compliance auditing, data privacy, or ABAC training.</li><li>
Medical Excellence Manager Experience</li></ul>
Why AstraZeneca:
Join a team that blends scientific rigor with commercial precision to launch innovations that matter to patients, moving from early diagnosis through treatment with an unwavering ethical core. We operate at pace in evolving markets with the freedom to experiment, learn, and improve, bringing surprising combinations of people together to spark bold thinking. We value kindness alongside ambition, and we follow the evidence to deliver solutions that serve patients and the business without compromising on doing the right thing. Your contribution will shape a connected healthcare ecosystem through partnerships and practical innovation, powered by a science-led pipeline that keeps learning fresh and impact real.
Call to Action:
Step forward to lead medical governance and excellence&mdash;bring your rigor and creativity to power faster, safer decisions and create meaningful patient impact!</div>

Nominated Signatory & Medical Excellence Lead

<div>
 
 Job Title: Nominated Signatory &amp; Medical Excellence Lead
 
 
 
 
 Introduction To Role
 
 
 
 Are you ready to uphold the highest standards of medical governance while accelerating field excellence to deliver better outcomes for patients? This role places you at the center of ethical decision-making and capability building, ensuring that every activity, material, and interaction reflects our standards and enables impact at pace.
 
 
 You will bridge rigorous compliance with practical execution, helping teams move fast and do the right thing. Can you translate strategy into measurable improvements that raise the quality and reach of medical engagement? Join us to combine science, ethics, and operational excellence in a dynamic environment where bold ideas and disciplined delivery go hand in hand.
 
 
 
 Accountabilities
 
 
 
 <ul>
 <li>
 Ethical Interactions Governance: Own and maintain local Ethical Interactions (EI) SOPs; translate global Code of Conduct into robust local procedures covering patient interactions, digital communications, diagnostics, patient affordability, and external funding.
 </li>
 <li>
 Nominated Signatory Leadership: Lead a team of risk assurance managers/signatories; review and approve materials and activities to meet ABAC, data privacy, local regulatory, and company standards; sign HCP/HCO agreements on behalf of the business.
 </li>
 <li>
 External Funding Oversight: Chair the Ethical Interactions Committee; assess, approve, and monitor external funding and third‑party engagements, ensuring transparency, fairness, and appropriate documentation.
 </li>
 <li>
 Risk and Assurance: Conduct first-line monitoring and quality checks; partner with Compliance and Assurance to execute risk assessments, define CAPAs, and track remediation to closure with evidence and sustainability plans.
 </li>
 <li>
 Medical Quality and Standards: Guide medical and marketing collaboration to ensure scientific accuracy, fair balance, and adherence to codes and SOPs across congresses, advisory boards, digital engagement, and field medical activities.
 </li>
 <li>
 Digital Compliance: Govern compliant HCP digital engagement platforms and content, ensuring consent, privacy-by-design, and appropriate content governance across channels.
 </li>
 <li>
 Process Improvement: Drive simplification and continuous improvement of governance processes, templates, and systems; embed controls proportionate to risk while enabling business agility.
 </li>
 <li>
 Cross-Functional Partnership: Advise cross‑functional teams on ethical and governance considerations for complex initiatives, mega events, and interactions with government officials.
 </li>
 <li>
 Medical Excellence: Purpose Elevate Medical Affairs capability across Egypt by defining competency standards, driving robust onboarding and continuous development for Medical Science Liaisons (MSLs) and Medical Advisors, and owning certification and quality assurance to improve scientific engagement, evidence generation readiness, and cross-functional impact.
 </li>
 <li>
 Liaise with the Global &amp; International Medical Excellence Team in connection to excellence programs, localize relevant initiatives to Egypt market as aligned with local strategy and compliance, and seek out opportunities for cross-market collaboration.
 </li>
 <li>
 Improve scientific engagement quality, call planning, narratives, objection handling, compliant interactions, and insight capture/translation.
 </li>
 <li>
 Equip medical managers with coaching requirements as per AZ standards.
 
 
 </li>
 </ul>
 
 Essential Skills/Experience
 
 
 
 <ul>
 <li>
 Education: Bachelor&rsquo;s degree in pharmacy or related life sciences field required.
 </li>
 <li>
 Experience: 7+ years in Medical Affairs/Compliance/Governance within pharma, including direct Nominated Signatory or equivalent approval authority.
 </li>
 <li>
 Expertise: Strong knowledge of ABAC, Data Privacy, EI codes, GxP fundamentals, and Egypt regulatory frameworks; audit and CAPA lifecycle management; digital engagement governance.
 </li>
 <li>
 Risk assessment, SOP authorship, stakeholder management, training design/delivery, analytical problem solving, change management, and clear written/oral communication in English
 
 
 </li>
 </ul>
 
 Desirable Skills/ Experience
 
 
 
 <ul>
 <li>
 Certifications : GCP/GVP quality, compliance auditing, data privacy, or ABAC training.
 </li>
 <li>
 Medical Excellence Manager Experience
 
 
 </li>
 </ul>
 
 Why AstraZeneca
 
 
 
 Join a team that blends scientific rigor with commercial precision to launch innovations that matter to patients, moving from early diagnosis through treatment with an unwavering ethical core. We operate at pace in evolving markets with the freedom to experiment, learn, and improve, bringing surprising combinations of people together to spark bold thinking. We value kindness alongside ambition, and we follow the evidence to deliver solutions that serve patients and the business without compromising on doing the right thing. Your contribution will shape a connected healthcare ecosystem through partnerships and practical innovation, powered by a science-led pipeline that keeps learning fresh and impact real.
 
 
 
 Call To Action
 
 
 
 Step forward to lead medical governance and excellence&mdash;bring your rigor and creativity to power faster, safer decisions and create meaningful patient impact!
 
 
 
 Date Posted
 
 
 
 08-مارس-2026
 
 
 
 Closing Date
 
 
 
 31-مارس-2026
 
 
 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.
</div>

Explore 1090+ Associate director medical affairs egypt in Egypt this March. Find roles across top companies and apply now to boost your career.

1090 associate director medical affairs egypt jobs In Egypt

Associate Director, Medical Affairs - Egypt

Patient Safety Center Associate Manager

Patient Safety Center Associate Manager

Corporate Affairs Expert

Nominated Signatory & Medical Excellence Lead

Nominated Signatory & Medical Excellence Lead

Nominated Signatory & Medical Excellence Lead