medical science liaison

Glenmark Pharmaceuticals

<div>
 
 
 
 Role Overview:
 
 
 
 
 
 
 
 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.
 
 
 
 
 
 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
 
 
 
 
 
 
 
 Job Responsibilities:
 
 
 
 
 
 
 <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>
 
 
 
 
 
 
 Educational Qualifications:
 
 
 
 
 
 
 
 Advanced degree in Life Sciences or Healthcare (PharmD, M. Pharm, PhD, Msc, MBBS, BDS or equivalent)
 
 
 
 
 
 
 
 Experience:
 
 
 
 
 
 
 
 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
 
</div>

Medical Science Liaison

Sanofi

<div>Job title: Medical Science Liaison &ndash; Oncology<ul><li>
Location: Riyadh, Saudi Arabia</li></ul>
About the job
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?
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.
About Sanofi
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.
Main responsibilities<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>
About you<ul><li>
Experience: Prior 3 years of experience in Medical Affairs within the pharmaceutical industry, with a background in Oncology and/or Multiple Myeloma being a strong advantage.</li><li>
Soft and technical skills: 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>
Education: University degree in life sciences; MD, PhD, or PharmD preferred.</li><li>
Languages: Fluency in Arabic and English required.</li></ul>
Why choose us?<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>
Pursue Progress. Discover Extraordinary.
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.
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.
null</div>

Medical Science Liaison Oncology

Meet Life Sciences

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

Medical Science Liaison (Oncology)

Baylor Miraca Genetics Laboratories LLC

<div>*** This candidate must reside in Florida, Georgia, South Carolina, or North Carolina

Medical Science Liaison

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.

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.

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.

QUALIFICATIONS AND EXPERIENCE:
<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>
Duties and Responsibilities:
<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>
PHYSICAL DEMANDS AND WORK ENVIRONMENT:
<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>
EEO Statement:

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.</div>

Medical Science Liaison- Southeast

Biogen

<div>About This Role
The Medical Science Liaison Pipeline Immunology is a 70 % field-based medical expert who drives strategic scientific engagement to support Biogen&rsquo;s pipeline development in GCC. This role is a SME who provides high-quality medical &amp; scientific support to key medical experts (KMEs) , delivers complex scientific presentations, and leads expert discussions. They work on medical core pillars: data dissemination, data generation and medical insight collections. The MSL Pipeline conducts analysis and selection to define the KME universe for the respective country and establishes robust KME networks to support pipeline objectives . Ultimately, the role serves to advance Biogen&rsquo;s pipeline strategy through expert engagement, medical education, and evidence and insights generation .
What You'll Do
<ul><li>As a SME d eliver s high-quality, complex medical presentations and lead scientific discussions with KMEs to t ranslate pipeline data into impactful content to inform clinical decision-making. Collects critical insights to inform local strategy.
</li><li>Disseminate innovative medical education materials and support internal training on disease areas and treatments to e nsure consistent, up-to-date knowledge across internal and external stakeholders.
</li><li>Stay current on therapy advances, research developments, and Biogen&rsquo;s products to m aintain scientific credibility and relevance in all engagements. Attends congresses and confere nce as needed.
</li><li>P rovide field-based medical support to KMEs in GCC to b uild trusted relationships and ensure accurate understanding of pipeline therapies.
</li><li>Collaborate cross-functionally with internal teams (e.g., sales, market access, pharmacovigilance) by sharing appropriately insights and executing on an aligned medical plan in line with the overall organizational goals.
</li><li>Organize and deliver medical education events and e nsure compliance with local regulations to promote informed clinical decision-making.
</li><li>Conduct analysis and selection to define the KME universe for GCC to i dentify and prioritize key experts for strategic engagement. Execute engagement plans as per plan.
</li><li>Establish and maintain KME networks to support pipeline objectives to f oster long-term partnerships that enhance medical insight and influence.
</li><li>In line with country strategy c ontribute to expanded access program (EAP) communications to f acilitate ethical and transparent access to investigational therapies.
</li><li>Ensure all activities comply with Biogen&rsquo;s Code of Business Conduct and local SOPs to u phold ethical standards and regulatory requirements in all interactions.
</li></ul>Who You Are
You are a highly motivated, field-driven MSL with strong Immunology expertise , energized by scientific exchange and spending the majority of your time engaging external stakeholders across Saudi Arabia and the GCC. You bring a collaborative, flexible mindset , navigating cross-functional environments with maturity, resilience, and a genuine willingness to contribute beyond formal boundaries.
Required Skills
<ul><li>7+ years of relevant experience in the pharmaceutical or biotechnology industry , including 2&ndash;4 years of experience as a Medical Science Liaison.
</li><li>Master&rsquo;s degree in Medical or Life Sciences is required ; advanced degrees such as M.D., Ph.D., or Pharm.D. are strongly preferred.
</li><li>Field-driven mindset , with the willingness to spend approximately 70% of time in the field , engaging external stakeholders and representing the pipeline regionally.
</li><li>Immunology experience is required , with the ability to confidently present complex scientific data and represent pipeline assets at a regional level.
</li><li>Strong scientific acumen with the ability to engage in high-level, evidence-based discussions with healthcare professionals and key medical experts.
</li><li>Working knowledge of cross-functional environments , including Regulatory Affairs, Drug Safety (PV), Market Access, Legal, and Compliance , with demonstrated flexibility in navigating cross-functional challenges.
</li><li>Experience in both Saudi Arabia and the broader Middle East (GCC) region is preferred , supporting effective regional engagement and growth.
</li><li>Willingness to travel up to 70% across the region.
</li><li>Fluency in English is required. 
</li></ul> 
Job Level: Management
<div><h2 class="jobSectionHeader"> 
Why Biogen?
</h2></div><div>We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&amp;I efforts.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.</div></div>

Medical Science Liaison Pipeline Immunology

Hikma

<div><div><div><div><div><div><div>Description:
Job 
Location: Dubai, United Arab Emirates. 
Department: Medical Affairs - Biotechnology 
Reports to: Associate Director, Medical 


Job Purpose:

The Sr MSL is a field-based medical expert role focused on developing and maintaining peer-to-peer relationships with key medical experts. This role will primarily support the company biotechnology franchise. The Sr MSL will collaborate with physicians and other medical experts to provide field observations to internal stakeholders and ensure that health care professionals have the most up to date information as the clinical development programs mature this role will be reporting to the MENA Medical Associate Director Biotechnology.

This is a field-based job with 80% of the time allocated to the field and nearly 20% travel time. 


Key Responsibilities:
<ul>
<li>Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the Biotechnology community.</li>
<li>Develop territory field medical plan and TLs Interaction plans based on therapeutic area objectives and TLs needs.</li>
<li>Support clinical development initiatives including site identification, trial recruitment, registry, and presentation of final approved data.</li>
<li>Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development.</li>
<li>Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders.</li>
<li>Support the medical community with up-to-date medical information, robust disease expertise, and product information.</li>
<li>Communicate clinical insights on new data to the company medical Affairs and to inform medical strategy for the assigned therapeutic area.</li>
<li>Train internal &amp; external stakeholders on key scientific and medical topics in relevant therapeutic area.</li>
<li>Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements.</li>
<li>Generate tactical regional plans to provide needs based, value-added support of the medical and scientific community in-line with company goals.</li>
<li>Uses systems to strategically map, identify, profile, and prioritize thought leaders in line with the medical plan and goals.</li>
<li>Maintain accurate reporting and documentation of MSL activities.</li>
<li>Provide medical and scientific information to respond to KOLs' technical questions about company`s product.</li>
<li>Lead meetings with KOLs to discuss relevant scientific literature and address their enquiries.</li>
<li>Make educational presentations to senior doctors and researchers, for example on clinical trial data.</li>
<li>Feed information back to marketing and sales colleagues to help develop marketing materials and commercial strategy.</li>
<li>Keep up to date with the latest scientific research and clinical data relevant to the company`s molecules.</li>
<li>Share safety information with the pharmacovigilance division.</li>
<li>Comply with all internal &amp; external regulations and codes that apply to medical, regulatory and compliance perspectives.</li>
<li>Support for the development of Medical Plans.</li>
<li>Support for management of clinical studies including Company Investigational Studies (CISs) &amp; Investigator Initiated Studies (IISs).</li>
<li>Supports product pre-launch, launch, and post-launch activities and communication plans within medical strategy and tactical plans.</li></ul> 


Qualifications &amp; Experience:
<ul>
<li>5-8 years of experience in the pharmaceutical industry.</li>
<li>A minimum of 2 years of experience in medical as MSL, Regulatory Affairs and/or Pharmacovigilance is preferred.</li>
<li>Business acumen courses/training is a plus.</li>
<li>Clinical research experience and GCP certification is a plus.</li>
<li>National experience is a Preferred.</li>
<li>Biotech experience is a plus.</li>
<li>Candidates must understand compliance considerations and demonstrate ability to work compliantly in a field-based role, within the medical organization, as well as across the commercial organization.</li>
</ul></div></div></div></div><div><div><div><div>Location:
Sharjah, AE</div></div></div></div></div></div></div>

Sr. Medical Science Liaison

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
MSL Position Summary 
 
MSLs embody our medical mission in becoming a trusted, agile partner who engages in relevant dialogue and delivers timely, high impact data and insights that advance the science or accelerate access, optimize medical practice and drive appropriate adoption of BMS medicines. The MSL role is a field-based role and it is anticipated that a MSL will spend their time in the field with external customers. 
 
The primary role of MSLs is to develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of interactions is to ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer-to-peer discussions aligned with medical strategies and needs expressed by the stakeholders. The scientific dialogue focuses on scientific/clinical information around disease management and BMS products in a fair and balanced way and includes appropriate Health Economics and Outcomes Research (HEOR) data. 
 
Position Responsibilities 
 
1. External Environment and Customer Focus
 
 
<ul><li>Develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1:1, group presentation; remote, etc.).</li></ul> 
<ul><li>Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.</li></ul> 
<ul><li>Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.</li></ul> 
<ul><li>Collect and provide meaningful medical insights back to the medical and commercial organization to be actioned in support of the strategy development.</li></ul> 
2. Contribute to the Medical Plan
 
 
<ul><li>Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs.</li></ul> 
<ul><li>Adopt institution/account planning approach and contribute to cross-functional institution/account plans.</li></ul> 
<ul><li>Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan</li></ul> 
3. Provide Medical Support
 
 
<ul><li>As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Market Access).</li></ul> 
<ul><li>Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers.</li></ul> 
4. Support Clinical Trial Activities
 
 
<ul><li>Support Interventional and Non-Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document.</li></ul> 
<ul><li>Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management.</li></ul> 
<ul><li>Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.</li></ul> 
<ul><li>Support HCPs in the ISR submission process as agreed with local medical management.</li></ul> 
5. Support Patient Safety Activities
 
 
<ul><li>Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.</li></ul> 

Degree Requirements 
 
<ul><li>Medical Doctor, Pharmacist</li></ul> 

Experience Requirements 
 
<ul><li>Working in a scientific and/or clinical research environment</li></ul> 
<ul><li>Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their patients</li></ul> 
<ul><li>Developing peer-to-peer relationships with TLs and other healthcare professionals</li></ul> 

Key Competency Requirements 
 
<ul><li>Ability to work independently and act as a team player</li></ul> 
<ul><li>Good communication and presentation skills to present scientific and/or clinical data to research or healthcare professionals</li></ul> 
<ul><li>Ability to quickly and comprehensively learn about new subject areas</li></ul> 
<ul><li>Disease area knowledge and an understanding of scientific publications</li></ul> 
<ul><li>Experience in Oncology disease area is a plus</li></ul> 
<ul><li>Knowledge of a scientific or clinical area</li></ul> 
<ul><li>Knowledge of clinical trial design and process</li></ul> 
<ul><li>Knowledge of the national healthcare and access environment</li></ul> 
<ul><li>Knowledge of HEOR core concepts</li></ul> 
<ul><li>Excellent English language skills (speaking and writing)</li></ul> 

Travel Required 
 
<ul><li>Travel required (varies by geography)</li></ul> 

Other 
 
<ul><li>Located in Ankara</li></ul> 
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
Supporting People with Disabilities 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
Candidate Rights 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Data Protection 
 
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 
 
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
R1599967 : Medical Science Liaison Oncology, Ankara</div>

Medical Science Liaison Oncology, Ankara

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