medical affairs specialist

AbbVie

<div><b>Company Description</b><p><br>
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.</p><b><br>
Job Description</b><p><b><br>
Affiliate:</b></p><p><b>
Gulf Levant
</b></p><p><b>Title:</b></p><p><b>
Medical Advisor &ndash; Gastroenterology
</b></p><p><b>Reporting to:</b></p><p><b>
Medical Manager &ndash; Immunology
</b></p><p><b>PRIMARY FUNCTION:
</b></p><p>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.</p><p><b>
RESPONSIBILITIES:</b></p><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><p></p><p><b><br>
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</b></p><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><p><b>
LOCATION:</b></p><p>
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field.</p><p></p><b><br>
Qualifications</b><br>
<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><br>
<b>
Additional Information</b><div></div><p><br>
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><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Medical Advisor

Boehringer Ingelheim

<p></p><div><p>We are looking for a <b>Medical Associate &amp; Regulatory Affairs Executive &ndash; Outsourced </b>, based in <b>Egypt </b>. This position will be responsible for executing local Regulatory Affairs (RA) and Medical Affairs activities in alignment with ROPU RA strategies and local business priorities, ensuring business continuity and compliance with internal and external regulations.<br>
</p><p></p><p>The role will support product registrations, regulatory intelligence, and medical affairs execution across assigned therapeutic areas, while collaborating closely with cross‑functional teams and external stakeholders. The objective of this position is to ensure timely regulatory compliance, effective medical activities execution, and strong stakeholder engagement in support of Boehringer Ingelheim&rsquo;s business objectives.
<br>
This position will be reporting to the relevant line manager within the organization.<br>
</p><p></p><p><b>Tasks &amp; Responsibilities:<br>
</b></p><p></p><p><b>Regulatory Affairs Activities:
</b></p><ul><li>Execute local Regulatory Affairs activities in line with ROPU RA strategies and defined timelines.
</li><li>Maintain product registrations and Regulatory Affairs databases to ensure business continuity and full compliance with internal and external regulations.
</li><li>Monitor and provide regular regulatory intelligence on changes in the regulatory environment and competitor activities, identifying potential risks and opportunities for the business.
</li><li>Ensure proactive and timely communication of relevant regulatory updates to internal stakeholders.
</li><li>Build and maintain strong working relationships with assigned regulatory authorities across OPU/cluster.
</li><li>Coordinate and collaborate effectively with regulatory service providers, local agents, and vendors.
</li>Execute agreed actions for assigned local Regulatory Affairs projects.<br>
<li>
</li></ul><p></p><p><b>Medical Affairs Activities:
</b></p><ul><li>Assist in the execution of all Medical Affairs activities related to Boehringer Ingelheim Medical Department.
</li><li>Oversee and monitor the medical budget allocated per product, ensuring all planned medical activities are executed efficiently and within the approved budget.
</li><li>Maintain accurate records of all medical approvals, expenses, and paid honoraria within the assigned OPU.
</li><li>Collect, consolidate, and prepare monthly feedback, reports, and summaries of Medical Affairs activities.
</li><li>Ensure proper documentation and archiving of all Medical Affairs-related materials and records.
</li>Ensure strict adherence to compliance requirements and Standard Operating Procedures (SOPs) in the execution of all medical activities.<br>
<li>
</li></ul><p></p><p><b>Stakeholder &amp; Cross‑Functional Collaboration:
</b></p><ul><li>Collaborate closely with cross‑functional teams including Medical Affairs, Marketing, Market Access, and Supply Chain to ensure alignment and effective implementation of business objectives.
</li>Support efficient communication and coordination with internal and external stakeholders to ensure timely delivery of regulatory and medical objectives.<br>
<li>
</li></ul><p></p><p><b>Requirements:
</b></p><p><b>Education:
</b></p><ul><li>Bachelor&rsquo;s degree in <b>Pharmacy
</b></li></ul><p><b>Experience &amp; Competencies:
</b></p><ul><li>Minimum <b>2&ndash;4 years of experience </b>in the pharmaceutical industry with a strong focus on Regulatory Affairs within a multinational organization.
</li><li>Previous experience with direct interactions with Regulatory Authorities is a strong asset.
</li><li>Ability to perform regulatory activities with high quality in a dynamic and fast‑changing environment.
</li><li>Strong organizational, communication, and cross‑functional collaboration skills.
</li>Ability to manage multiple priorities while ensuring compliance and timely execution of deliverables.<br>
<li>
</li></ul><p></p><p><b>What happens Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your CV. If we see a match, we will invite you for a screening interview.
<br>
<br>
<b>SPL Screening:
</b></p><p>In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</p></div>

Medical Associate & Regulatory Affairs Executive

<div>
 We are looking for a
 <strong>
  Medical Associate &amp; Regulatory Affairs Executive &ndash; Outsourced
 </strong>
 , based in
 <strong>
  Egypt
 </strong>
 . This position will be responsible for executing local Regulatory Affairs (RA) and Medical Affairs activities in alignment with ROPU RA strategies and local business priorities, ensuring business continuity and compliance with internal and external regulations.
 <br/>
 <br/>
 The role will support product registrations, regulatory intelligence, and medical affairs execution across assigned therapeutic areas, while collaborating closely with cross‑functional teams and external stakeholders. The objective of this position is to ensure timely regulatory compliance, effective medical activities execution, and strong stakeholder engagement in support of Boehringer Ingelheim&rsquo;s business objectives.
 <br/>
 <br/>
 This position will be reporting to the relevant line manager within the organization.
 <br/>
 <br/>
 <strong>
  Tasks &amp; Responsibilities:
  <br/>
  <br/>
 </strong>
 <strong>
  Regulatory Affairs Activities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Execute local Regulatory Affairs activities in line with ROPU RA strategies and defined timelines
  </li>
  <li>
   Maintain product registrations and Regulatory Affairs databases to ensure business continuity and full compliance with internal and external regulations
  </li>
  <li>
   Monitor and provide regular regulatory intelligence on changes in the regulatory environment and competitor activities, identifying potential risks and opportunities for the business
  </li>
  <li>
   Ensure proactive and timely communication of relevant regulatory updates to internal stakeholders
  </li>
  <li>
   Build and maintain strong working relationships with assigned regulatory authorities across OPU/cluster
  </li>
  <li>
   Coordinate and collaborate effectively with regulatory service providers, local agents, and vendors
  </li>
  <li>
   Execute agreed actions for assigned local Regulatory Affairs projects
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Medical Affairs Activities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist in the execution of all Medical Affairs activities related to Boehringer Ingelheim Medical Department
  </li>
  <li>
   Oversee and monitor the medical budget allocated per product, ensuring all planned medical activities are executed efficiently and within the approved budget
  </li>
  <li>
   Maintain accurate records of all medical approvals, expenses, and paid honoraria within the assigned OPU
  </li>
  <li>
   Collect, consolidate, and prepare monthly feedback, reports, and summaries of Medical Affairs activities
  </li>
  <li>
   Ensure proper documentation and archiving of all Medical Affairs-related materials and records
  </li>
  <li>
   Ensure strict adherence to compliance requirements and Standard Operating Procedures (SOPs) in the execution of all medical activities
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Stakeholder &amp; Cross‑Functional Collaboration:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Collaborate closely with cross‑functional teams including Medical Affairs, Marketing, Market Access, and Supply Chain to ensure alignment and effective implementation of business objectives
  </li>
  <li>
   Support efficient communication and coordination with internal and external stakeholders to ensure timely delivery of regulatory and medical objectives
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements:
  <br/>
  <br/>
 </strong>
 <strong>
  Education:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Pharmacy
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience &amp; Competencies:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum 2&ndash;4 years of experience in the pharmaceutical industry with a strong focus on Regulatory Affairs within a multinational organization
  </li>
  <li>
   Previous experience with direct interactions with Regulatory Authorities is a strong asset
  </li>
  <li>
   Ability to perform regulatory activities with high quality in a dynamic and fast‑changing environment
  </li>
  <li>
   Strong organizational, communication, and cross‑functional collaboration skills
  </li>
  <li>
   Ability to manage multiple priorities while ensuring compliance and timely execution of deliverables
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What happens Next?
  <br/>
  <br/>
 </strong>
 We are looking forward to receiving your application! We will then have a look at your CV. If we see a match, we will invite you for a screening interview.
 <br/>
 <br/>
 <strong>
  SPL Screening:
  <br/>
  <br/>
 </strong>
 In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.
 <br/>
 <br/>
 Our Company
 <br/>
 <br/>
 <strong>
  Why Boehringer Ingelheim?
  <br/>
  <br/>
 </strong>
 With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.
 <br/>
 <br/>
 Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
 <br/>
 <br/>
 Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
 <br/>
 <br/>
 Want to learn more? Visit https://www.boehringer-ingelheim.com
</div>


MSD GCC

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 A world-class Medical Affairs organization is critical to our Company&rsquo;s mission to save and improve lives. It is committed to advancing medical practice through the proper implementation of our innovative drugs and vaccines with a vision to be the most trusted, science-driven and patient-committed medical affairs organization in the industry and a mission to communicate and generate medical evidence to help those responsible for health-care decisions make informed choices that improve access and health outcomes for patients around the world.
 <br/>
 <br/>
 We are looking for
 <strong>
  Gulf Oncology Medical Advisor,
 </strong>
 who will be responsible for local Oncology Franchise Medical Strategy &amp; Planning, local Scientific Leader and Key Decision Makers engagement and planning, collaborative activities with local Oncology Societies/Scientific community, local Promotional &amp; Non-promotional compliance for Oncology activities, materials &amp; programs, Medical Training.
 <br/>
 <br/>
 <strong>
  Major Responsibilities
  <br/>
  <br/>
 </strong>
 Medical activities
 <br/>
 <br/>
 <ul>
  <li>
   Ensure regular scientific updating for cross-functional team.
  </li>
  <li>
   Provide medical input including patient flow analysis to the assigned tumor types
  </li>
  <li>
   Proactively communicate the science behind our Company&rsquo;s Oncology portfolio to scientific leaders in terms of locally registered products &amp; reactively respond to their queries on our Company&rsquo;s pipeline.
  </li>
  <li>
   Providing medical/scientific robust support with full collaboration with Policy &amp; Access to facilitate formulary inclusions/ reimbursement.
  </li>
  <li>
   Ensure regular scientific updating for Sales &amp; Marketing team.
  </li>
  <li>
   Construct &amp; execute valuable scientific education activities to position our Company as a partner to the oncology scientific community
  </li>
  <li>
   Conduct input seeking activities (ex Group Input Meetings) for proper understanding of local epidemiology &amp; management patterns across indications, according to our Company&rsquo;s, local &amp; international compliance guidelines/regulations.
  </li>
  <li>
   Conducts medical training to the Oncology Commercial, Market Access, Sales &amp; Regulatory functions.
  </li>
  <li>
   Ensures all Oncology promotional &amp; non promotional activities/programs in Gulf countries are executed in a compliant manner according to Company&rsquo;s regulations/codes/SOPs in adherence with Local &amp; International compliance regulations/standards.
   <br/>
   <br/>
  </li>
 </ul>
 Clinical Research, Local Data Generation and Pharmacovigilance
 <br/>
 <br/>
 <ul>
  <li>
   Supports Clinical research &amp; local data generation activities for Global, regional &amp; local studies
  </li>
  <li>
   Identification of appropriate local sites / investigators for Oncology clinical research programs.
  </li>
  <li>
   Ensures timely reporting of adverse events &amp; assists local Pharmacovigilance team in assessment &amp; completion of required data for optimal reporting.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Physician, Dentist or Pharmacist educational or working background.
  </li>
  <li>
   Oncology/Hematology experience is highly preferred.
  </li>
  <li>
   Gulf experience is highly preferred.
  </li>
  <li>
   1+ years experienced in Medical Affairs department in multinational pharma companies.
  </li>
  <li>
   Arabic &amp; English Fluency.
  </li>
  <li>
   Good utility of Microsoft Office (Word, PowerPoint &amp; Excel).
  </li>
  <li>
   Excellent Communication Skills &amp; ability to engage with Scientific Leaders, Key Decision Makers in a confident high-level scientific rapport.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Location
 </strong>
 Dubai
 <br/>
 <br/>
 <strong>
  Required Skills
  <br/>
  <br/>
 </strong>
 Hematology, Medical Affairs, Medical Research, Medical Training, Medical Writing, Oncology, Oncology Marketing, Pharmaceutical Industry, Project Management, Scientific Communications, Scientific Publications, Strategic Networking, Strategic Thinking
 <br/>
 <br/>
 <strong>
  Preferred Skills
  <br/>
  <br/>
 </strong>
 Current Employees apply HERE
 <br/>
 <br/>
 Current Contingent Workers apply HERE
 <br/>
 <br/>
 <strong>
  Search Firm Representatives Please Read Carefully
  <br/>
  <br/>
 </strong>
 Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, 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.
 <br/>
 <br/>
 <strong>
  Employee Status
  <br/>
  <br/>
 </strong>
 Regular
 <br/>
 <br/>
 <strong>
  Relocation
  <br/>
  <br/>
 </strong>
 No relocation
 <br/>
 <br/>
 <strong>
  VISA Sponsorship
  <br/>
  <br/>
 </strong>
 Yes
 <br/>
 <br/>
 <strong>
  Travel Requirements
  <br/>
  <br/>
 </strong>
 10%
 <br/>
 <br/>
 <strong>
  Flexible Work Arrangements
  <br/>
  <br/>
 </strong>
 Not Applicable
 <br/>
 <br/>
 <strong>
  Shift
  <br/>
  <br/>
 </strong>
 Not Indicated
 <br/>
 <br/>
 <strong>
  Valid Driving License
  <br/>
  <br/>
 </strong>
 Yes
 <br/>
 <br/>
 <strong>
  Hazardous Material(s)
  <br/>
  <br/>
 </strong>
 n/a
 <br/>
 <br/>
 <strong>
  Job Posting End Date
  <br/>
  <br/>
 </strong>
 03/6/2026
 <br/>
 <br/>
 <ul>
  <li>
   A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requisition ID
 </strong>
 R386631
</div>


Gulf Oncology Medical Advisor

<div><b>Site Name:</b> Riyadh Olaya Towers<br>
<b>Posted Date:</b> Feb 10 2026<p><b><br>
Job Purpose:</b></p><ul><li>
The Medical Scientific Liaison (MSL) is a non-promotional field-based medical role responsible for conducting medical engagements/activities that ensure the safe and effective use of GSK&rsquo;s medicines while generating medical insights.</li><li>
MSLs are expected to drive EEs/HCPs education journeys using the AKU/ADoPT tool, provide support to GSK clinical development &amp; Key Evidence Generation programs.</li></ul><p></p><p><b>
Key Responsibilities:</b></p><p></p><ul><li>
Provide product and disease area information to external experts. This need is met primarily through direct scientific interactions with external experts and healthcare professionals, including proactive data presentations and reactive responses to medical information queries.</li></ul><p></p><ul><li>
MSLs are field-based scientific experts in specific therapeutic areas, clinical practice, and competitor landscape. Through his/her expertise and external interactions he/she will gather insights which will assist in the development and execution of innovative Medical Affairs strategies and plans that clearly support GSK development of medicines of value for patients.</li></ul><p></p><ul><li>
The language and activities of the MSL must always reflect the medical nature of the role, be fair, balanced, scientific and evidence based. MSLs may be required to manage scientific engagement budget, train internal stakeholders and contribute in medical affairs and/or R&amp;D activities.</li></ul><p></p><p><b>
MSLs responsibilities include:</b></p><p></p><p><i>
Collect &amp; generate insights:
</i></p><ul><li>Conduct proactive/reactive (1:1), (1: many) discussions and meetings, support advisory boards/consultations and scientific workshops.</li><li>
Use GSK tools to capture insights and medical voice of customers while regularly assessing related KPIs and their impact on TA strategic objectives</li><li>
Attend scientific meetings/congresses</li></ul><p></p><p><i>
Inform decisions:
</i></p><ul><li>Provide product and TA information to internal and External customers.</li><li>
Conduct Medical Education programs. (GSK led, collaborative or supported)</li><li>
Map evidence gaps &amp; collaborate in developing evidence generation plans</li><li>
Support patients access to GSK brands</li><li>
Engage &amp; represent medical with EE, payers, government &amp; formularies</li></ul><p></p><p>
Change behavior:</p><ul><li>
Work collaboratively to scale EE ADoPT level in the assigned TA</li><li>
Engage proactively/reactively (according to Asset local registration status) to update TA related guidelines and educate HCPs about them</li><li>
Transform guidelines into execution protocols</li><li>
Address HCP&rsquo;s unsolicited questions regarding GSK products within the Medical Affairs/scientific/Medical Information booth</li></ul><p></p><p><b>
Knowledge, Skills &amp; Competencies:</b></p><ul><li>
Pharmaceutical science degree (Saudi National is preferred)</li><li>
At least 2-year experience as a Med rep. Therapy Area experience is preferred (Cardiovascular and Metabolic).</li><li>
Proven successful track record.</li><li>
Having a valid license from the Saudi Commission for Health Specialties</li><li>
Ability to analyze, present and discuss scientific data in the therapeutic area with external and internal stakeholders</li><li>
High level of discipline, ability to organize the activity and to reasonably use the working time within the established independence limits.</li><li>
Developed skills in business planning, business orientation and working under a dynamically changing condition</li><li>
Fluent in professional English language. Arabic language is an advantage.</li></ul><p></p><p><b>
#LI-Remote</b></p><p></p><p><b>
Why GSK?</b><br>
<b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.</p><p></p><p>
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>
Contact information:</b><br>
You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>
Important notice to Employment businesses/ Agencies</b></p><p>
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p></div>

Medical Science Liaison Vaccines

Galderma

<div><div>Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.</div><div></div><div><br>
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.</div><div></div><div><br>
At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.</div><div></div><div>
Job Title: Medical Scientific Liaison (MSL)<br>
Location: Dubai</div><div></div><div>
With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology. For this purpose, the Medical Scientific Liaison (MSL) is a key internal expert, providing a field-based scientific and clinical support to healthcare professionals to maintain a high level of medical, scientific and technical knowledge and expertise in relation to Dermatology &amp; Aesthetics with a focus in UAE (KSA as needed support.)</div><ul><li><div>
Play a key role in successfully launching new treatment options for treating various dermatoses and support A&amp;C</div></li><li><div>
Support and facilitated field force education and training to ensure seamless implementation of medical strategies</div></li><li><div>
Act as the primary point of contact for new products in therapeutic dermatology and A&amp;C business (including internal and external medical-scientific projects, non-interventional and investigator-initiated trials - IIT)</div></li><li><div>
Building relationships and maintaining very close contact with medical experts and local representatives of scientific societies, 80 % of time allocated to field activities.</div></li><li><div>
Collaborate with the team to implement medical-scientific strategies, focusing on developing central/key strategies for clinical studies and other projects</div></li><li><div>
Establish strong cross-departmental relationships, working closely with medical office/affairs staff, marketing teams, and sales teams</div></li><li><div>
Actively participate in congresses, staying updated with the latest findings in relevant indication areas and market trends while providing expert insights to the organization</div></li></ul><div></div><div>
Key Responsibilities:</div><div>
Strategic Goals</div><ul><li><div>
Advance science and standards of care for patients and healthcare providers.</div></li><li><div>
Enhance Galderma&rsquo;s scientific credibility with national and regional key thought leaders (KTLs/KOLs).</div></li><li><div>
Act as the main point of contact for KTLs/KOLs to facilitate medical-scientific projects, clinical studies, NIS, and investigator-initiated trials (IITs).</div></li><li><div>
Identify, develop and maintain contact with local, regional and national KTLs/KOLs and experts through internally approved field engagement plans</div></li><li><div>
Develop and maintain collaborative relationships with KTLs/KOLs and academic centers in the therapeutic area to ensure access to current medical and scientific information and to facilitate Galderma research and educational priorities and strategic initiatives</div></li></ul><div></div><div>
Information &amp; Support</div><ul><li><div>
Ensure that KTLs/KOLs can access all the practical and clinically relevant information and solutions they need to use Galderma&rsquo;s products efficiently and safely</div></li><li><div>
Interact with, and support the needs of, Tier 1, 2 and 3 external experts</div></li><li><div>
Work to communicate information and facilitate dialogue about Gladerma&rsquo;s compound in development (Nemolizumab) in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, Galderma&rsquo;s policies and procedures and accepted standards of best practice</div></li><li><div>
Independent organization and implementation of advisory boards</div></li><li><div>
Carry out and support sales force education and training courses</div></li><li><div>
Deliver credible scientific and medical Slide kits to physicians, healthcare providers and other stakeholders as needed</div></li><li><div>
Attend relevant scientific meetings and conferences</div></li><li><div>
Support scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific and medical information</div></li><li><div>
As appropriate and needed; produce, review, and update internally approved scientific presentations for assigned therapeutic areas</div></li><li><div>
Maintain a high level of scientific knowledge to ensure credible dissemination of scientific information and informed scientific dialogue with KOLs/KTLs</div></li><li><div>
Gather and generate actionable insights through: Attending congresses, engaging with external stakeholders, staying updated in relevant scientific literature, preparing summaries, and presenting key perspectives to Galderma teams including competitor analyses</div></li></ul><div></div><div>
Collaboration &amp; Communication</div><ul><li><div>
Close interdepartmental cooperation with the medical office staff and relevant marketing &amp; sales teams</div></li><li><div>
Support internal teams such as sales and marketing to develop their scientific expertise through the delivery of scientific update presentations</div></li><li><div>
Work collaboratively and cross-functionally with other in-field members while retaining functional independence</div></li><li><div>
Communicate and interact with the Global and International Medical Affairs teams</div></li><li><div>
Serve as a point of contact within the Medical Affairs Team for KTLs/KOLs within the UAE in order to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant Galderma medicines, to support their safe, effective and appropriate use</div></li><li><div>
Participate in the selection process to identify appropriately qualified thought leaders Galderma would wish to engage in collaborative efforts &ndash; such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.) while ensuring a high level of scientific or educational integrity in these collaborative efforts</div></li></ul><div></div><div>
Compliance &amp; Legal Guidance</div><ul><li><div>
Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, Galderma&rsquo;s policies and accepted standards of best practices</div></li><li><div>
Support Galderma research by identifying investigators, undertaking scientific exchange and providing feedback and insight to medical and clinical teams</div></li><li><div>
Respond to unsolicited requests for medical and scientific information</div></li><li><div>
Utilize modern technology platforms to maximize efficiency and effectiveness and limit travel requirements. Ensure the integrity of the scientific data used in promotional claims and materials, if requested</div></li><li><div>
Adhere to all company policies and procedures including but not limited to Code of Conduct, fleet, IT and confidentiality</div></li><li><div>
Other duties as assigned by management.</div></li></ul><div></div><div>
Qualifications &amp; Skills:</div><ul><li><div>
Medical, Pharmacy, or higher degree (e.g., MSc, PhD) in Life sciences.</div></li><li><div>
Dermatology, Aesthetics, or Immunology-Biologics experience is desirable.</div></li><li><div>
Several years of relevant medical, research, or pharmaceutical/biotech experience preferred.</div></li><li><div>
Experience liaising with medical professionals and opinion leaders.</div></li><li><div>
Proven ability to develop and present scientific/medical content to diverse audiences.</div></li><li><div>
Strong communication and presentation skills.</div></li><li><div>
Skilled in meeting planning, facilitation, and technical platforms.</div></li><li><div>
Ability to work effectively in a team-oriented, matrix environment.</div></li><li><div>
Highly organized, able to prioritize, and adapt in a dynamic environment.</div></li><li><div>
Ability to build credibility and relationships with medical professionals.</div></li><li><div>
English: spoken and written as a second language for scientific purposes</div></li></ul><div></div><div>
Our people make a difference</div><div>
At Galderma, you&rsquo;ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.</div></div><div></div>

Medical Scientific Liaison (MSL) - UAE

EAZYMED TECHNOLOGIES PRIVATE LIMITED

<p>Role: Manager - Medical Affairs &amp; Programs</p><p><b>Location: Bengaluru</b></p><p>About MrMed</p><p>MrMed is redefining access to life‑saving super‑speciality medicines in India. We&rsquo;re building the country&rsquo;s most trusted digital pharmacy for complex therapies, making treatments more accessible, affordable, and reliable for patients across every corner of India.</p><p>By combining technology, logistics, and medical expertise, we simplify everything from medicine access to patient education with empathy and precision. Our mission is simple: to bridge the gap between speciality care and those who need it most.</p><p>The Opportunity</p><p>We&rsquo;re looking for a doctor who&rsquo;s ready to move beyond clinical practice and shape the next chapter of healthcare delivery in India.</p><p>As Manager - Medical Affairs &amp; Programs, you&rsquo;ll sit at the intersection of medicine, technology, and business, bringing clinical depth to strategic decisions while helping us scale new programs that improve patient outcomes.</p><p>This is a role for someone who wants to build, lead, and influence, not just execute.</p><p>What You&rsquo;ll Lead</p><ul><li><b>Medical Content &amp; Education:</b> Design and review accurate, credible medical content and learning modules for patients, doctors, and partners.</li><li><b>Compliance &amp; Governance:</b> Own the medical compliance process for medicines and patient services; ensure all initiatives meet the highest clinical and ethical standards.</li><li><b>Consultation Programs:</b> Help architect the operations and workflows for virtual doctor consultations, setting up best practices and ensuring compliance.</li><li><b>Cross-Functional Impact:</b> Collaborate with marketing, operations, and product teams to bring medical insight into brand narratives, processes, and decisions.</li></ul><p>What You&rsquo;ll Bring</p><ul><li>MBBS (mandatory); higher qualifications in pharmacology, healthcare management, or digital health are a plus.</li><li>Strong interest in healthcare systems, strategy, or business operations.</li><li>Excellent communication and storytelling skills, written and verbal.</li><li>Detail-oriented, structured thinker with execution bias.</li><li>Entrepreneurial mindset and genuine curiosity about how healthcare businesses scale.</li></ul><p>Why MrMed</p><ul><li>Shape how India accesses and experiences specialty medicines.</li><li>Work with a passionate team that blends medicine, tech, and empathy.</li><li>Build a career path that combines clinical expertise with strategic execution.</li><li>Be part of a fast-growing startup at the frontier of healthcare innovation.</li></ul><p>If you&rsquo;re a doctor ready to rewrite how medicine meets business, this is your stage.</p><p>Apply now and help us build the future of specialty healthcare.</p><p>Share your resume to hr@mrmed.in</p><p>Job Types: Full-time, Permanent</p><p>Pay: ₹35,000.00 - ₹40,000.00 per month</p><p>Benefits:</p><ul><li>Health insurance</li><li>Provident Fund</li></ul><p>Application Question(s):</p><ul><li>Have you completed MBBS</li></ul><p>Work Location: In person</p>

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