medical scientific liaison

AstraZeneca

<div>
 <strong>
  Job Title:
 </strong>
 <strong>
  Medical Scientific Liaison / Medical Advisor (Cairo / Giza)
  <br/>
  <br/>
 </strong>
 <strong>
  Introduction to role
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  Accountabilities
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Essential Skills/Experience
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Desirable Skills/Experience
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </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.
 <br/>
 <br/>
 <strong>
  Date Posted
  <br/>
  <br/>
 </strong>
 09-مارس-2026
 <br/>
 <br/>
 <strong>
  Closing Date
  <br/>
  <br/>
 </strong>
 09-أبريل-2026
 <br/>
 <br/>
 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>


Medical Scientific Liaison / Medical Advisor (Cairo / Giza)

Baylor Miraca Genetics Laboratories LLC

<div><p><b>*** This candidate must reside in Florida, Georgia, South Carolina, or North Carolina</b></p>
<p><b>
Medical Science Liaison</b></p>
<p>
The field-based Medical Affairs team of Medical Science Liaisons (MSLs) at Baylor Genetics play a key role in clinical and scientific education to internal and external parties. The MSL serves as a scientific and clinical expert and liaison between Baylor Genetics and key opinion leaders (KOLs), healthcare professionals, medical associations and academic centers through the development, dissemination and clarification of pertinent scientific and clinical information. Each MSL establishes long-term clinical and science-based relationships with healthcare professionals that help to ensure access to current, accurate and relevant scientific information through the process of education via one-on-one interactions, small group discussions, and presentations at local and national conferences. The MSL will aid other members of the Medical Affairs team in development of scientific content, and the MSL is responsible for organizing and delivering continuing education (CME/CEU) presentations.</p>
<p>
The MSL may also collaborate with various external agencies, consultants, investigators, and collaborators as well as internal stakeholders, including Sales, Customer Support, Business Development, Product, Marketing, and Research/Development. The MSL also serves as an expert resource on Baylor Genetics products and associated disease states.</p>
<p>
MSLs are expected to work closely with the Manager of Medical Affairs and the Science Writer &amp; Content Manager to contribute to multiple abstracts and publications each year. To be successful in this role, this individual will be a strategic thinker with excellent attention to detail, outstanding oral and written communication skills, and a demonstrated ability to communicate complex scientific concepts in a compelling and concise manner to various internal and external stakeholders. This position can be remote.</p>
<p><b>
QUALIFICATIONS AND EXPERIENCE:</b></p>
<ul>
<li>Advanced degree in scientific field required (MS in Genetic Counseling, PhD, NP, MD).</li>
<li>Minimum of 3+ years of clinical experience in pediatric medicine with an emphasis on genetics required. In addition, 2+ years of industry experience in Medical Affairs strongly preferred.</li>
<li> Familiarity with key aspects of genomics and molecular diagnostics technologies.</li>
<li> Proven history delivering high quality scientific presentations.</li>
<li>Proven history of authoring peer-reviewed scientific publications, scientific posters &amp; abstracts.</li>
<li>Fluency with all MS Office and SharePoint software required.</li>
<li>Experience leading initiatives and/or teams cross functionally.</li>
<li> Excellent planning and organizational skills with excellent verbal and written communication skills.</li>
<li>Ability to efficiently manage time and priorities.</li>
<li>Ability to work in a fast-paced environment while working collaboratively on multiple projects with competing priorities.</li>
<li>Demonstrated problem solving skills in a complex and matrixed environment.</li>
<li>Self-driven attitude to take initiative and work independently and collaboratively with minimal supervision towards a common goal.</li>
<li>Ability to read, interpret, and convey complex scientific information to audiences of varying backgrounds.</li>
<li>This position requires 40-50% travel (national and international), including overnight and occasional weekend travel.</li>
<li> Attendance at periodic internal and external meetings which may include national and international locations.</li>
</ul>
<p><b>Duties and Responsibilities:</b></p>
<ul>
<li>Work with a motivated and dynamic Medical Affairs team to provide educational support to healthcare professionals and organizations on Baylor Genetics products and services.</li>
<li> Work with contacts outside of the company including healthcare providers, investigators and collaborators, influential clinicians, KOLs (Key Opinion Leaders), and advisory boards, as appropriate.</li>
<li> Serve as an expert resource on pediatric genetics &amp; genomics and on Baylor Genetics products to provide educational support for the field sales team and other internal partners.</li>
<li> With the broader Medical Affairs team, participate in abstract development and support publication efforts, as well as attend relevant educational meetings and conferences annually.</li>
<li> In collaboration with product marketing and scientific communications, develop multi-channel medical educational activities and tools including illustrative case studies, speaker programs, slide decks, CE events, etc.</li>
<li> Work effectively and collaboratively with internal sales, marketing, and customer support to support sales colleague development through coaching aligned with technical and business opportunities/strengths. Review sales materials for technical accuracy, medical appropriateness and utility to customers and field team.</li>
<li> Deliver effective, high-quality presentations in scientific venues, online webinars, etc.</li>
<li> Monitor and analyze medical literature to inform internal stakeholders of key scientific and competitive developments.</li>
<li> Attend assigned major medical conferences to provide scientific support to the commercial Baylor Genetics team and contribute to a meeting summary report from each conference to summarize key scientific and competitive observations for internal stakeholders.</li>
<li>Lead and contribute to other Medical Affairs projects as needed.</li>
<li> May perform other related duties as required and/or assigned.</li>
</ul>
<p><b>PHYSICAL DEMANDS AND WORK ENVIRONMENT:</b></p>
<ul>
<li>Frequently required to talk or hear.</li>
<li>Frequently required to utilize visual acuity to operate equipment, read technical information, and/or use a keyboard.</li>
<li>Frequently required to sit or stand.</li>
</ul>
<p><b>EEO Statement:</b></p>
<p>
Baylor Genetics is proud to be an equal-opportunity employer dedicated to building an inclusive and diverse workforce. We do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, gender identity, veteran status, disability, genetic information, pregnancy, childbirth, or related medical conditions, or any other status protected under applicable federal, state, or local law.</p></div><p></p>

Medical Science Liaison- Southeast

Glenmark Pharmaceuticals

<div>
 <p>
  <strong>
   <u>
    Role Overview:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Medical Science Liaison (MSL) &ndash; Oncology is a field-based medical professional responsible for executing Glenmark&rsquo;s medical affairs strategy in the region assigned for oncology products across their lifecycle, including pipeline and marketed assets.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Working in close alignment with Global Medical Affairs and the local cross-functional team, the MSL serves as a scientific expert and trusted partner to oncologists, hematologists, investigators, and other key healthcare stakeholders. The role focuses on high-quality, non-promotional scientific exchange, medical insight generation, and support of evidence generation initiatives, while ensuring full compliance with local regulations, including local regulatory requirements and the Code of Conduct
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Responsibilities:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Identifies, maps, and develops scientific relationships with key oncology KOLs, investigators, and cancer centers across regions assigned in alignment with the medical strategy.
  </li>
  <li>
   Conducts high-quality, non-promotional scientific exchange with HCPs, ensuring fair-balanced communication of clinical data, benefits, risks, and appropriate use of Glenmark oncology products.
  </li>
  <li>
   Gathers, analyses, and communicates actionable medical insights from the field to inform local and global medical strategies.
  </li>
  <li>
   Supports planning and execution of medical education initiatives such as advisory boards, medical education programs (MEPs), and focused group discussions.
  </li>
  <li>
   Supports clinical evidence generation activities including investigator-initiated studies, real-world evidence initiatives, and company-sponsored studies in collaboration with Global Medical and Clinical teams.
  </li>
  <li>
   Maintains in-depth knowledge of disease areas, treatment paradigms, competitive landscape, and local treatment guidelines relevant to assigned oncology assets
  </li>
  <li>
   Provides scientific training and medical input to internal stakeholders, including sales and cross-functional teams, ensuring accuracy and compliance.
  </li>
  <li>
   Attends local and regional oncology congresses and scientific meetings to remain current on emerging data and evolving standards of care.
  </li>
  <li>
   Responds to unsolicited medical information requests in a timely, accurate, and compliant manner, in collaboration with Medical Information and PV teams.
  </li>
  <li>
   Ensures all medical activities are conducted in compliance with Glenmark SOPs, health authority regulations, and the local code of conduct
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Educational Qualifications:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Advanced degree in Life Sciences or Healthcare (PharmD, M. Pharm, PhD, Msc, MBBS, BDS or equivalent)
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Experience:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Minimum 2&ndash;4 years of experience as a Medical Science Liaison, preferably in Oncology. Experience engaging with oncology stakeholders within the country healthcare system is strongly preferred. Familiarity with local regulatory requirements, clinical research processes, and medical affairs operations
 </p>
</div>


Medical Science Liaison

Novartis

<div>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 <strong>
  Medical Expert Engagement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).
  </li>
  <li>
   Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Scientific Information &amp; Requests
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.
  </li>
  <li>
   Involve HCPs in advisory boards, educational activities, and publications when relevant.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Clinical Research Support
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.
  </li>
  <li>
   Facilitate IIT submissions and material transfer agreements for independent research.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Scientific Exchange &amp; Insights
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Promote scientific exchange on emerging principles and trends.
  </li>
  <li>
   Collect and report HCP insights to inform medical strategy and IPS planning.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Internal Contributions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Act as a local medical resource for disease area and product training.
  </li>
  <li>
   Contribute to IPS and Medical Affairs strategy design and execution.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compliance &amp; Integrity
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).
  </li>
  <li>
   Foster a diverse, inclusive, and harassment-free environment.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education &amp; Communication
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide scientific and educational information to HCPs on patient-critical issues.
  </li>
  <li>
   Support internal capability building through training and knowledge sharing.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A degree in PharmD, PhD, MD (Medical Doctor) is essential.
  </li>
  <li>
   At least 2-year experience as Medical Science Liaison, specific experience in Oncology is a plus.
  </li>
  <li>
   Fluent in both Arabic and English languages.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why Novartis:
 </strong>
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
 <br/>
 <br/>
 <strong>
  Benefits and Rewards:
 </strong>
 Learn about all the ways we&rsquo;ll help you thrive personally and professionally.
 <br/>
 <br/>
 Read our handbook (PDF 30 MB)
 <br/>
 <br/>
</div>


Senior Medical Science Liaison - Oncology

<div><div><h3 class="jobSectionHeader"><b>Summary
</b></h3><div>To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.<br>
<br>
#LI-onsite</div>
</div><div><h3 class="jobSectionHeader"><b>About the Role
</b></h3><div><h3 class="jobSectionHeader"><b>Medical Expert Engagement</b></h3><ul><li>
Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).</li><li>
Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.</li></ul><h3 class="jobSectionHeader"><b>
Scientific Information &amp; Requests</b></h3><ul><li>
Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.</li><li>
Involve HCPs in advisory boards, educational activities, and publications when relevant.</li></ul><h3 class="jobSectionHeader"><b>
Clinical Research Support</b></h3><ul><li>
Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.</li><li>
Facilitate IIT submissions and material transfer agreements for independent research.</li></ul><h3 class="jobSectionHeader"><b>
Scientific Exchange &amp; Insights</b></h3><ul><li>
Promote scientific exchange on emerging principles and trends.</li><li>
Collect and report HCP insights to inform medical strategy and IPS planning.</li></ul><h3 class="jobSectionHeader"><b>
Internal Contributions</b></h3><ul><li>
Act as a local medical resource for disease area and product training.</li><li>
Contribute to IPS and Medical Affairs strategy design and execution.</li></ul><h3 class="jobSectionHeader"><b>
Compliance &amp; Integrity</b></h3><ul><li>
Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).</li><li>
Foster a diverse, inclusive, and harassment-free environment.</li></ul><h3 class="jobSectionHeader"><b>
Education &amp; Communication</b></h3><ul><li>
Provide scientific and educational information to HCPs on patient-critical issues.</li><li>
Support internal capability building through training and knowledge sharing.</li></ul><p></p><p><b>
Minimum Requirements</b></p><ul><li>
A degree in PharmD, PhD, MD (Medical Doctor) is essential.</li><li>
At least 2-year experience as Medical Science Liaison, specific experience in Oncology is a plus.</li><li>
Fluent in both Arabic and English languages.</li></ul></div><p></p>
</div><div><div><p><b>Why Novartis:</b> Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture</p><p><b>
Benefits and Rewards:</b> Learn about all the ways we&rsquo;ll help you thrive personally and professionally.<br>
Read our handbook (PDF 30 MB)</p></div></div></div>
<br><div><div>Division
<div>International
</div></div><div>Business Unit
<div>Development
</div></div><div>Location
<div>Saudi Arabia
</div></div><div>Site
<div>Jeddah
</div></div><div>Company / Legal Entity
<div>SA01 (FCRS = SA001) Novartis Saudi Arabia Ltd
</div></div><div>Functional Area
<div>Research &amp; Development
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No
</div></div><div></div><div><div><div><div><div>VIDEO</div>
</div>
</div></div></div><div></div><div><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</p></div></div>

Meet Life Sciences

<div>
 <p>
  <strong>
   Field-Based | Dubai, UAE
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  I&rsquo;m currently supporting a
  <strong>
   pharmaceutical client
  </strong>
  with the search for several
  <strong>
   Medical Science Liaison (MSL) &ndash; Oncology
  </strong>
  hires in
  <strong>
   Dubai, UAE
  </strong>
  .
 </p>
 <p>
  <br/>
 </p>
 <p>
  This is a field-based opportunity for scientifically strong medical professionals who enjoy building credible relationships with external experts and supporting high-quality scientific exchange across oncology products spanning both
  <strong>
   marketed and pipeline assets
  </strong>
  .
 </p>
 <p>
  Working closely with global and local cross-functional teams, these individuals will act as trusted scientific partners to
  <strong>
   oncologists, haematologists, investigators, and other key stakeholders
  </strong>
  across their assigned regions. The roles will focus on
  <strong>
   non-promotional scientific engagement, insight gathering, and support for evidence-generation activities
  </strong>
  , while ensuring all work is delivered compliantly and in line with local regulations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Key responsibilities
 </p>
 <ul>
  <li>
   Identify, map, and develop scientific relationships with
   <strong>
    key opinion leaders, investigators, and cancer centres
   </strong>
   across the assigned territory
  </li>
  <li>
   Deliver
   <strong>
    high-quality, balanced, non-promotional scientific exchange
   </strong>
   with healthcare professionals across the oncology landscape
  </li>
  <li>
   Gather and share
   <strong>
    field medical insights
   </strong>
   to help inform local and global medical strategy
  </li>
  <li>
   Support the planning and execution of
   <strong>
    advisory boards, medical education programmes, and scientific discussions
   </strong>
  </li>
  <li>
   Contribute to
   <strong>
    evidence-generation initiatives
   </strong>
   , including investigator-initiated studies, real-world evidence activities, and company-sponsored research
  </li>
  <li>
   Maintain up-to-date knowledge of
   <strong>
    disease areas, treatment pathways, clinical data, competitive activity, and local treatment guidelines
   </strong>
  </li>
  <li>
   Provide scientific input and training to relevant
   <strong>
    internal cross-functional stakeholders
   </strong>
  </li>
  <li>
   Attend
   <strong>
    regional and local congresses / scientific meetings
   </strong>
   to stay current on emerging data and evolving standards of care
  </li>
  <li>
   Respond to
   <strong>
    unsolicited medical information requests
   </strong>
   in a timely, accurate, and compliant manner
  </li>
  <li>
   Ensure all activities are carried out in line with
   <strong>
    internal procedures, local regulations, and applicable codes of conduct
   </strong>
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  External stakeholder exposure
 </p>
 <ul>
  <li>
   Oncologists
  </li>
  <li>
   Haematologists
  </li>
  <li>
   Allied Healthcare Professionals
  </li>
  <li>
   National and Regional KOLs
  </li>
  <li>
   Investigators and Academic Institutions
  </li>
  <li>
   Oncology Societies and Co-operative Groups
  </li>
  <li>
   Patient Advocacy Groups
  </li>
  <li>
   CROs and external partners
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Ideal background
 </p>
 <p>
  I&rsquo;d be keen to speak with candidates who bring:
 </p>
 <ul>
  <li>
   Previous experience in an
   <strong>
    MSL or field medical role
   </strong>
  </li>
  <li>
   Strong scientific understanding of
   <strong>
    oncology
   </strong>
   , with haematology exposure also of interest
  </li>
  <li>
   Experience engaging with
   <strong>
    KOLs, investigators, and specialist healthcare professionals
   </strong>
  </li>
  <li>
   A strong grounding in
   <strong>
    medical affairs
   </strong>
   and compliant scientific communication
  </li>
  <li>
   The ability to interpret and communicate
   <strong>
    clinical data
   </strong>
   clearly and credibly
  </li>
  <li>
   Strong relationship-building and cross-functional collaboration skills
  </li>
  <li>
   A proactive approach and willingness to travel across the assigned region
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  If this could be of interest, get in touch for a confidential discussion or send me your cv at kenneth.ubaldo@meetlifesciences.com
 </p>
 <p>
 </p>
</div>


Medical Science Liaison (Oncology)

Sanofi

<div><p><b>Job title: </b>Medical Science Liaison &ndash; Oncology</p><ul><li><b>
Location</b>: Riyadh, Saudi Arabia</li></ul><p></p><p><b>
About the job</b></p><p>
As Medical Science Liaison &ndash; Oncology within our Specialty Care team, you'll serve as a trusted scientific partner to key oncology stakeholders, bridging cutting-edge clinical insights with real-world medical practice. Ready to get started?</p><p>
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.</p><p></p><p><b>
About Sanofi</b></p><p>
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.</p><p></p><p><b>
Main responsibilities</b></p><ul><li>
Build and maintain trusted scientific relationships with Key Opinion Leaders (KOLs) and healthcare professionals to advance understanding of oncology therapy areas, including Multiple Myeloma.</li><li>
Provide accurate, balanced, and timely medical information to healthcare professionals and decision-makers in response to clinical inquiries.</li><li>
Collaborate with Medical Affairs and clinical teams to support Real-World Evidence studies, Phase IV clinical projects, Investigator-Sponsored Studies (ISS), and site selection for clinical trials.</li><li>
Serve as a scientific resource for the commercial team, supporting objection handling and acting as a therapy area expert.</li><li>
Actively represent Sanofi at key medical and scientific conferences, staffing medical information booths and gathering competitive intelligence.</li><li>
Receive, report, and transmit adverse events in line with company pharmacovigilance procedures, and ensure Risk Management Plan implementation.</li><li>
Uphold compliance, ethical leadership, and safety standards in all field activities.</li></ul><p><b>
About you</b></p><ul><li><b>
Experience</b>: Prior 3 years of experience in Medical Affairs within the pharmaceutical industry, with a background in <b>Oncology and/or Multiple Myeloma </b>being a strong advantage.</li><li><b>
Soft and technical skills</b>: Strong scientific communication skills with the ability to engage KOLs and cross-functional stakeholders at all levels; knowledge of clinical research methodology and GCP; business acumen and self-motivation; collaborative team player with strong planning and decision-making abilities.</li><li><b>
Education</b>: University degree in life sciences; MD, PhD, or PharmD preferred.</li><li><b>
Languages</b>: Fluency in Arabic and English required.</li></ul><p><b>
Why choose us?</b></p><ul><li>
Join the team transforming care for patients with some of the highest unmet needs &mdash; including rare cancers and immune-mediated diseases &mdash; and be part of delivering hope where it matters most.</li><li>
Work at the intersection of science and patient impact, engaging directly with leading oncology KOLs and shaping the future of cancer care in the region.</li><li>
Grow your career in a cross-functional environment with access to global Medical Affairs expertise, international mobility, and continuous development opportunities.</li><li>
Be part of a company that invests in you &mdash; with structured career paths, mentoring, and a culture that values bold thinking and scientific excellence.</li><li>
Thrive in an inclusive, purpose-driven workplace where your contributions directly improve patients' lives across Saudi Arabia and beyond.</li><li>
Enjoy a comprehensive rewards package including healthcare benefits and flexible working arrangements.</li></ul><p><b>
Pursue Progress. Discover Extraordinary.</b></p><p>
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary &ndash; together.</p><p>
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.</p>
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