medical advisor

Novo Nordisk, Inc.

<div><div><div><div><div>Medical Advisor
</div></div></div></div><div><div><div><div>Category: Medical Affairs
</div></div></div></div><div><div><div><div>Location:
Karachi, Sindh, PK 
</div></div></div></div><div></div><div><div><div><div><div>Are you a talented and dedicated medical doctor looking for a job in the pharmaceutical industry? Are you passionate about medical science and eager to make a difference in the diabetes community as well as building strong relationships with key stakeholders? If so, we invite you to apply for the position of Medical Advisor at Novo Nordisk Pakistan. Read more and apply today for a life-changing career.</div>
<div>
Your new role</div>
<div>
As a Medical Advisor at Novo Nordisk, you will play a pivotal role in shaping and executing medical strategies to support our diabetes and obesity portfolios.</div>
<div>
Your responsibilities will be:</div>
<ul><li>Develop and drive the medical strategy to align with and support the overarching brand and business priorities.</li></ul>
<ul><li>Facilitate KOL engagement in trials, identify new sites, conduct site education visits, support investigator-sponsored studies, and develop relationships with Key Opinion Leaders (KOLs) for speaker engagements.</li></ul>
<ul><li>Develop and conduct advisory boards, communicate scientific and clinical data, create and execute publication plans for assigned portfolios, present at national and international conferences, and engage external authors.</li></ul>
<ul><li>Develop and implement the medical education strategy for assigned portfolios; review all commercial-led medical education meetings and accredited medical education; attend conferences and congresses.</li></ul>
<ul><li>Conduct internal training; translate scientific information for internal stakeholders to assist with the development and implementation of strategy; approve promotional material; provide tailored medical responses.</li></ul>
<div>
Your new department 
The Medical Affairs Team at Novo Nordisk Pakistan is based in Karachi and is part of the MRPV (Medical, Regulatory, and Pharmacovigilance) department. We are a dynamic and collaborative team dedicated to ensuring the optimal delivery of scientific information to the medical community. Our mission is to drive medical strategies, support the diabetes and obesity portfolios, and make a meaningful difference in the lives of patients. Working closely with key stakeholders, we foster a fast-paced and innovative environment where your contributions will directly impact our success.</div>
<div>
Your skills &amp; qualifications 
We are looking for candidates who meet the following qualifications:</div>
<ul>
<li>MBBS degree</li>
<li>Minimum 2 years&rsquo; experience in Medical Affairs Department</li>
<li>Advanced English proficiency</li>
<li>Ready for business travel</li>
</ul>
<div>Working at Novo Nordisk 
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.</div>
<div>
Deadline 
27.03.2026. Applications are reviewed on an ongoing basis.</div>
<div>
Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.</div>
<div>
Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.</div><div>
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.</div> 
<div></div>
<div>
At Novo Nordisk, we're not chasing quick fixes &ndash; we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger &ndash; a legacy of impact that reaches far beyond today.</div></div></div></div></div></div>

Medical Advisor

Novo Nordisk

<div>
 Are you a talented and dedicated medical doctor looking for a job in the pharmaceutical industry? Are you passionate about medical science and eager to make a difference in the diabetes community as well as building strong relationships with key stakeholders? If so, we invite you to apply for the position of
 
 Medical Advisor
 
 at Novo Nordisk Pakistan. Read more and apply today for a life-changing career.
 
 
 
 Your new role
 
 
 
 As a Medical Advisor at Novo Nordisk, you will play a pivotal role in shaping and executing medical strategies to support our diabetes and obesity portfolios.
 
 
 
 Your Responsibilities Will Be
 
 
 
 <ul>
 <li>
 Develop and drive the medical strategy to align with and support the overarching brand and business priorities.
 </li>
 <li>
 Facilitate KOL engagement in trials, identify new sites, conduct site education visits, support investigator-sponsored studies, and develop relationships with Key Opinion Leaders (KOLs) for speaker engagements.
 </li>
 <li>
 Develop and conduct advisory boards, communicate scientific and clinical data, create and execute publication plans for assigned portfolios, present at national and international conferences, and engage external authors.
 </li>
 <li>
 Develop and implement the medical education strategy for assigned portfolios; review all commercial-led medical education meetings and accredited medical education; attend conferences and congresses.
 </li>
 <li>
 Conduct internal training; translate scientific information for internal stakeholders to assist with the development and implementation of strategy; approve promotional material; provide tailored medical responses.
 
 
 </li>
 </ul>
 
 Your new department
 
 
 
 The Medical Affairs Team at Novo Nordisk Pakistan is based in Karachi and is part of the MRPV (Medical, Regulatory, and Pharmacovigilance) department. We are a dynamic and collaborative team dedicated to ensuring the optimal delivery of scientific information to the medical community. Our mission is to drive medical strategies, support the diabetes and obesity portfolios, and make a meaningful difference in the lives of patients. Working closely with key stakeholders, we foster a fast-paced and innovative environment where your contributions will directly impact our success.
 
 
 
 Your Skills &amp; Qualifications
 
 
 
 We are looking for candidates who meet the following qualifications:
 
 
 <ul>
 <li>
 MBBS degree
 </li>
 <li>
 Minimum 2 years&rsquo; experience in Medical Affairs Department
 </li>
 <li>
 Advanced English proficiency
 </li>
 <li>
 Ready for business travel
 
 
 </li>
 </ul>
 
 Working at Novo Nordisk
 
 
 
 Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.
 
 
 
 Deadline
 
 
 
 27.03.2026. Applications are reviewed on an ongoing basis.
 
 
 Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.
 
 
 Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.
 
 
 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
 
 
 At Novo Nordisk, we're not chasing quick fixes &ndash; we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger &ndash; a legacy of impact that reaches far beyond today.
</div>

AstraZeneca

<div>Title
Medical Advisor, CVRM
Job Description
Field Medical Advisor is responsible for providing high quality medical &amp; scientific expertise via in-depth expert medical and scientific product/disease area discussions and presentations of detailed clinical data in a non-promotional scientific context.
This role will be responsible for a highly strategic product that will involve working extensively with external Health Care professionals to forge strong relations KEEs and developing strong advocates to support education in respective therapeutic area in UAE.
This role will be also accountable for sharing KEE&rsquo;s insights to the brand team meetings and provide input for the development of company&rsquo;s Medical and Brand plans.
Typical Accountabilities
Build, enhance, maintain with scientific leaders (KEEs)<ul><li>
Provide AZ with an understanding of the local medical community, clinical practice trends, HCP insight and real or perceived gaps in current scientific knowledge and medical treatment</li><li>
Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective and balanced way.</li><li>
Responsible for identifying and developing scientifically based relationships with UAE KEEs.</li><li>
Work with HCPs as partners in scientific activities that help advance disease understanding and are consistent with Medical Affairs strategy &amp; objectives, such as:
Interact in the field with the medical community in the context of various medical projects such as clinical trials, Non-Interventional Studies, Investigator Sponsored Studies (ISSs), scientific exchange.
 Identify potential speakers and train speakers as appropriate for local events
Provide recommendations for advisory board / round table discussion participants and serve as faculty/facilitators for advisory board meetings.
Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.
Facilitate continuing medical education events for HCPs.</li></ul>
Build or Initiate scientific programs to explore unmet medical needs in priority disease area(s) through obtaining and sharing valuable insights<ul><li>
Provide actionable insights that enhance the value and appropriate use of AZ products and disease management to internal stakeholders</li><li>
Engage in strategic planning meetings with payer customers or hospital decision makers where the discussion of scientific topics is clearly separated from discussion of promotional and/or other business topics.</li><li>
Demonstrate expertise and knowledge of AZ products, emerging therapies, competitors, patient and treatment trends, clinical trials, and scientific activities within the Disease Area and continuously updates this expertise and knowledge based on training direction and approved resources provided.</li><li>
Support the Medical Manager and Marketing Team in development of non-promotional and promotional materials/programs.</li></ul>
Act as scientific expert in priority disease area for internal stakeholders<ul><li>
Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.</li><li>
Provide the AZ internal stakeholders with an understanding of the local medical community, clinical practice, trends and real or perceived gaps in current scientific knowledge and medical treatment, competitor information</li><li>
Provide scientific support at AZ sponsored educational events</li><li>
Gather, monitor and share competitor knowledge that may affect company strategies</li><li>
Planning and executing regional medical activities during the product launch processes.</li></ul>
Medical Background Training<ul><li>
Serve as a medical resource for the sales representatives and accurately answer any medical question they may have to help them utilize their approved materials and to help them understand therapeutic area.</li><li>
Participate/develop/conduct therapeutic area and product trainings and periodic scientific updates to the internal customers</li></ul>
Medical Information<ul><li>
Respond to unsolicited requests for information about unapproved AZ products or unapproved uses of approved products, presenting such information in an objective, well balanced, substantiated manner that is scientific in tone and content, free of promotional messages, truthful, and is not misleading</li><li>
Demonstrate appropriate response and documents the provision of accurate, scientific data in response to unsolicited scientific questions posed by healthcare providers with Company Policies, and applicable laws, regulations and ethical standards.</li></ul>
Operates in:
Own country 
Essential
For External Candidates:<ul><li>
Minimum of 2 years&rsquo; experience in Medical Affairs role in pharmaceutical industry.</li><li>
Established track record of basic or clinical research</li></ul>
For Internal Candidates:<ul><li>
Minimum of 2 years&rsquo; Medical Affairs experience is required within AstraZeneca with strong performance record.</li></ul>
For All Candidates:<ul><li>
Bachelor&rsquo;s degree in medicine, Pharmacy, Pharmacology or degree in biomedical sciences</li><li>
Excellent ability to learn and acquire scientific concepts and knowledge.</li><li>
Demonstrated expertise in synthesizing scientific information and communicating it effectively at peer level with HCPs.</li><li>
Ability to work in matrix multicultural organizations and collaborate effectively with commercial counterparts</li><li>
Exceptional English communication skills both oral and written as a need to deliver comprehensive presentations and facilitate discussions with small/large groups of health care providers and internal management</li><li>
Excellent problem-solving ability in addition to strong negotiation skills.</li><li>
Ability to demonstrate good business judgment.</li><li>
High sense of urgency and commitment to excellence in the successful achievement of objectives.</li><li>
Excellent planning and organizational skills to demonstrate leadership and initiative and demonstrated ability to work in a self-directed manner.</li></ul>
Desirable<ul><li>
Experience with CVRM is preferable.</li><li>
Postgraduate degree would be an advantage.</li><li>
Current familiarity with healthcare environment, including opinion leaders, academia, the medical community and related dynamics in UAE market.</li><li>
Other relevant pharmaceutical industry experience or previous clinical experience as an HCP (pharmacist, doctor) is preferable.</li><li>
Established track record of basic or clinical research.</li></ul>
Key Relationships to reach solutions
Internal (to AZ or team)<ul><li>
Medical Team</li><li>
Access Team</li><li>
Regulatory Team</li><li>
Marketing Team</li><li>
Commercial Team</li><li>
Pharmacovigilance Team</li><li>
Medical Excellence &amp; operation Team</li></ul>
External (to AZ)<ul><li>
Key Opinion Leaders</li><li>
Key Decision Makers</li><li>
Health Care Professionals</li><li>
Clinical Investigators / Research Experts</li><li>
Professional Associations and Societies</li><li>
Patient Associations</li></ul></div>

Medical Advisor, CVRM

<div>Job Title: Medical Advisor Oncology (Breast Cancer)
Introduction to role
Here you&rsquo;ll have the opportunity to make a meaningful difference to patients&rsquo; lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines &ndash; for the world&rsquo;s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem. With our ground-breaking pipeline, the outlook is bright. Be proud to be part of a place that has achieved so much yet is still moving forward. There&rsquo;s no better time to join our global, growing enterprise as we lead the way for healthcare and society.
Accountabilities:
In this role, you will deliver AstraZeneca's updated medical information to healthcare professionals through various channels. You will efficiently manage clinical studies, ensuring they meet quality, cost, and time standards, and provide monitoring services from start to finish. You will plan and complete projects, delivering progress reports as needed. Additionally, you will contribute to team development by sharing knowledge and coaching. You will ensure patient safety and compliance with adverse event reporting standards and manage the provision of named patient supplies in line with regulatory and ethical obligations. Lastly, you will coordinate pharmacovigilance systems to meet regulatory requirements and AstraZeneca standards. Expect to spend 80% of your time in the field.
Essential Experience:<ul><li>
Bachelor&rsquo;s degree in pharmacy / medicine.</li><li>
3&ndash;4 years of experience in a medical or scientific role within the pharmaceutical industry</li><li>
Experience working within a multinational pharmaceutical environment</li><li>
Fluency in spoken and written English</li></ul>
Desirable Skills/Experience<ul><li>
Breast Cancer experience</li><li>
Ability to interact with and manage a range of stakeholders both internally and externally</li><li>
Knowledge of legislation relevant to Pharmaceutical Ecosystem</li><li>
Deep interest in and understanding science</li><li>
Strong collaborator and reflects strong influence capability</li></ul>
At AstraZeneca, we change the practice of medicine and improve the patient&rsquo;s experience by generating and communicating compelling medical evidence. We translate our wealth of medical and scientific expertise to ensure that the data we produce helps physicians better treat patients at every point in their journey. Our culture is one of openness and transparency, fused with ambition and drive. We work seamlessly and inclusively across teams, roles, and levels to leverage our diverse skills and go further together. Join us in our mission to redefine cancer treatment and make a significant impact on patients' lives.</div>

Medical Advisor - Oncology (Breast Cancer)

<div>
 
 Job Title: Medical Advisor Oncology (Breast Cancer)
 
 
 
 
 Introduction to role
 
 
 
 Here you&rsquo;ll have the opportunity to make a meaningful difference to patients&rsquo; lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines &ndash; for the world&rsquo;s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem. With our ground-breaking pipeline, the outlook is bright. Be proud to be part of a place that has achieved so much yet is still moving forward. There&rsquo;s no better time to join our global, growing enterprise as we lead the way for healthcare and society.
 
 
 
 Accountabilities
 
 
 
 In this role, you will deliver AstraZeneca's updated medical information to healthcare professionals through various channels. You will efficiently manage clinical studies, ensuring they meet quality, cost, and time standards, and provide monitoring services from start to finish. You will plan and complete projects, delivering progress reports as needed. Additionally, you will contribute to team development by sharing knowledge and coaching. You will ensure patient safety and compliance with adverse event reporting standards and manage the provision of named patient supplies in line with regulatory and ethical obligations. Lastly, you will coordinate pharmacovigilance systems to meet regulatory requirements and AstraZeneca standards. Expect to spend
 
 80% of your time in the field
 
 .
 
 
 
 Essential Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in pharmacy / medicine.
 </li>
 <li>
 3&ndash;4 years of experience in a medical or scientific role within the pharmaceutical industry
 </li>
 <li>
 Experience working within a multinational pharmaceutical environment
 </li>
 <li>
 Fluency in spoken and written English
 
 
 </li>
 </ul>
 
 Desirable Skills/Experience
 
 
 
 <ul>
 <li>
 Breast Cancer experience
 </li>
 <li>
 Ability to interact with and manage a range of stakeholders both internally and externally
 </li>
 <li>
 Knowledge of legislation relevant to Pharmaceutical Ecosystem
 </li>
 <li>
 Deep interest in and understanding science
 </li>
 <li>
 Strong collaborator and reflects strong influence capability
 
 
 </li>
 </ul>
 At AstraZeneca, we change the practice of medicine and improve the patient&rsquo;s experience by generating and communicating compelling medical evidence. We translate our wealth of medical and scientific expertise to ensure that the data we produce helps physicians better treat patients at every point in their journey. Our culture is one of openness and transparency, fused with ambition and drive. We work seamlessly and inclusively across teams, roles, and levels to leverage our diverse skills and go further together. Join us in our mission to redefine cancer treatment and make a significant impact on patients' lives.
 
 
 
 Date Posted
 
 
 
 12-مارس-2026
 
 
 
 Closing Date
 
 
 
 22-أبريل-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>

AbbVie

<div>Company Description 
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 &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. 
Job Description 
Affiliate:
Gulf Levant
Title:
Medical Advisor &ndash; Gastroenterology
Reporting to:
Medical Manager &ndash; Immunology
PRIMARY FUNCTION:
Represent the affiliate&rsquo;s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic area(s). Provide medical / scientific expert advice / guidance to key customers for assigned product(s) and relevant therapeutic area(s), including scientific exchange and professional relationship development with External Experts (EEs). Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross-functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.
RESPONSIBILITIES:<ul><li>
Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.</li><li>
Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.</li><li>
Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).</li><li>
Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.</li><li>
Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.</li><li>
Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)</li><li>
Deliver training to sales forces and other departments; develop and update relevant training materials.</li><li>
Clinical Research Activities:<ul><li>
Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).</li><li>
Provide the required oversight to manage review, approval and conduct of IIS studies.</li><li>
Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).</li></ul></li><li>
Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie&rsquo;s internal policies and guidelines and in accordance with local laws.</li><li>
Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie&rsquo;s policies and procedures and accepted standards of best practice.</li><li>
Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.</li><li>
Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.</li><li>
Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.</li><li>
Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.</li></ul> 
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:<ul><li>
In-Field/Brand Team members (as applicable)</li><li>
Affiliate R&amp;D personnel: Medical Director, Medical operation and Evidence Generation Specialist, Medical Managers/Advisors; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel (as applicable)</li><li>
Marketing and Sales of assigned product and therapeutic area; Market access teams; Affiliate Brand teams.</li><li>
Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC.</li><li>
Area and HQ based Therapeutic Area medical affairs teams.</li><li>
Area Medical Affairs teams</li><li>
Medical Directors and Clinical Teams within Clinical Development Operations and Global Medical Affairs.</li><li>
Healthcare personnel (including physicians, nurses, pharmacists).</li><li>
Participating Research Investigators; thought leaders/external experts.</li><li>
Institutions and Scientific or Medical Societies.</li><li>
Hospitals, other healthcare providers, payers, and Local Regulatory Authorities.</li></ul>
LOCATION:
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field. 
Qualifications 
<ul><li>
Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered</li><li>
Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.</li><li>
Prior experience in Medical Affairs is required.</li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li><li>
Ability to comprehensively learn about new subject areas and environments.</li><li>
Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.</li><li>
A good understanding of written and oral English is mandatory.</li><li>
Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.</li><li>
Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage.</li><li>
Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate&rsquo;s medical and clinical activities as necessary.</li><li>
Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.</li><li>
High customer orientation and high digital savviness skills.</li><li>
Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>
Ability to travel regularly (approximately 50%)</li></ul> 

Additional Information<div></div> 
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.
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html</div>

Medical Advisor Immunology – Gastroenterology Gulf

<div>
 
 Job Title:
 
 
 Medical Scientific Liaison / Medical Advisor (Cairo / Giza)
 
 
 
 
 Introduction to role
 
 
 
 Here you&rsquo;ll have the opportunity to make a meaningful difference to patients&rsquo; lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines &ndash; for the world&rsquo;s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes, and shaping the patient ecosystem. With our ground-breaking pipeline, the outlook is bright. Be proud to be part of a place that has achieved so much yet is still moving forward. There&rsquo;s no better time to join our global, growing enterprise as we lead the way for healthcare and society.
 
 
 
 Accountabilities
 
 
 
 <ul>
 <li>
 Medical Information Leadership: Deliver AstraZeneca&rsquo;s updated medical information to healthcare professionals across multiple channels, ensuring accuracy, relevance, and timely engagement that supports better clinical decisions.
 </li>
 <li>
 Clinical Study Management: Plan, initiate, and manage clinical studies to agreed quality, cost, and time standards; provide full monitoring services from start to finish to maintain scientific integrity and operational excellence.
 </li>
 <li>
 Project Delivery: Define scope, set milestones, and complete projects; provide clear, concise progress reports that drive alignment and enable swift, informed decisions.
 </li>
 <li>
 Team Development and Coaching: Share knowledge and coach colleagues to strengthen team capability, building consistent ways of working and elevating scientific standards.
 </li>
 <li>
 Patient Safety and Compliance: Ensure patient safety and uphold adverse event reporting standards in all interactions and activities, embedding compliance into daily practice.
 </li>
 <li>
 Named Patient Supply Governance: Manage the provision of named patient supplies in line with regulatory and ethical obligations, ensuring appropriate access and documentation.
 </li>
 <li>
 Pharmacovigilance Coordination: Coordinate pharmacovigilance systems to meet regulatory requirements and AstraZeneca standards, ensuring robust, timely safety oversight
 
 
 </li>
 </ul>
 
 Essential Skills/Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in Pharma / Medical
 </li>
 <li>
 At least Three Years of experience in a multinational environment
 </li>
 <li>
 At least One Year of experience as MSL / Medical Advisor
 </li>
 <li>
 Fluency in spoken and written English language
 </li>
 <li>
 Cardiovascular / Renal / Metabolic Experience
 
 
 </li>
 </ul>
 
 Desirable Skills/Experience
 
 
 
 <ul>
 <li>
 Pharmaceutical experience is an asset
 </li>
 <li>
 Working towards MD/PHD
 </li>
 <li>
 Ability to interact and manage a range of stakeholders both internally and externally
 </li>
 <li>
 Knowledge of legislation relevant to Pharmaceutical Ecosystem
 </li>
 <li>
 Deep interest and understanding of science
 </li>
 <li>
 Strong collaborator and reflects strong influence capability
 </li>
 <li>
 Possess effective communication and facilitation skills
 
 
 </li>
 </ul>
 At AstraZeneca, we change the practice of medicine and improve the patient experience by generating and communicating compelling medical evidence. We translate our wealth of medical and scientific expertise to ensure that the data we produce helps physicians better treat patients at every point in their journey. Our culture is one of openness and transparency, fused with ambition and drive. We work seamlessly and inclusively across teams, roles, and levels to leverage our diverse skills and go further together. Join us in our mission to redefine cancer treatment and make a significant impact on patients' lives.
 
 
 
 Date Posted
 
 
 
 09-مارس-2026
 
 
 
 Closing Date
 
 
 
 09-أبريل-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.
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