At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
The Medical Science Liaison (MSL), Oncology – Melanoma and GI Tumors, is responsible for engaging in peer-to-peer scientific dialogue with Regional Thought Leaders (RTLs), National Thought Leaders, and Healthcare Professionals (HCPs) within an assigned geography. This role translates scientific data into clinical insights to support patient care and ensure the safe and effective use of Bristol Myers Squibb (BMS) therapies.
The MSL serves as a clinical and scientific advisor to cross-functional partners, provides field-based medical insights, and supports pre- and peri-launch activities aligned to the medical strategy. This is a field-based role requiring significant external engagement with investigators, healthcare professionals, and thought leaders.
Key Responsibilities
Medical Engagement
Develop and maintain trusted relationships with academic and community Thought Leaders through high-quality scientific exchange
Engage in proactive and reactive scientific dialogue to inform medical strategy and support product lifecycle management
Deliver educational presentations and scientific updates in both individual and group settings (in-person and virtual)
Collaborate with medical societies, patient advocacy groups (PAGs), and guideline committees
Provide training and support for external speakers as needed
Support payer engagement alongside cross-functional partners during pre- and peri-launch phases
Address unsolicited medical inquiries, including off-label questions, through in-person and virtual “Medical on Call” engagements
Utilize digital tools and platforms to enhance engagement and effectiveness
Capture and document field insights and achieve defined annual goals
Clinical Trial Engagement
Provide insights to clinical development teams on study and site feasibility based on field expertise
Maintain relationships with investigators and support clinical trial awareness and participation
Identify and assess potential research sites to support interventional and non-interventional studies
Support investigator-sponsored research (ISR) processes and follow-up activities
Lead and support clinical evidence communications, including major data readouts (e.g., Phase 3 results)
Ensure compliance with pharmacovigilance requirements, including reporting of adverse events
Collaborate with Global Development Operations (GDO) and home office medical teams
Cross-Functional Collaboration
Serve as a scientific expert and advisor to internal stakeholders
Partner across matrix teams (e.g., Medical, HEOR, Commercial) to align on strategy
Support equitable access to clinical trials across healthcare systems
Represent BMS with integrity and compliance in all external interactions
Required Qualifications & Experience
Advanced scientific or clinical degree (MD, PharmD, PhD, NP, PA, or equivalent)
Demonstrated experience in a scientific, clinical, or research environment
Strong experience in oncology required (GI preferred)
Field medical experience preferred
Deep understanding of Thought Leader engagement and healthcare landscape
Knowledge of: Clinical trial design and execution
Scientific publications and data interpretation
Pharmaceutical compliance and regulatory requirements
Healthcare systems and patient access dynamics
Key Competencies
Scientific Agility
Ability to communicate complex scientific data clearly and effectively
Strong understanding of clinical practice, treatment paradigms, and competitive…