Medical Science Liaison, Oncology – GI, Breast, Melanoma

Bristol Myers Squibb

. Engage in peer-to-peer scientific dialogue with Regional Thought Leaders, National Thought Leaders, and Healthcare Professionals within an assigned geography .

Posted 10/14/2026full-timeRemote • Michigan • United StatesMid-LevelSenior💰 $168,220 - $203,837 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in oncology and clinical trial design, with a strong ability to engage Thought Leaders and healthcare professionals. Proficient in translating scientific data into actionable insights while ensuring compliance with regulatory requirements.

Highest-signal resume keywords

Oncology ExpertiseClinical Trial DesignThought Leader EngagementData Analysis and InterpretationDigital Engagement Platforms

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Advanced Scientific DegreeClinical Research ExperienceKnowledge of Pharmaceutical ComplianceUnderstanding of Patient Access DynamicsAbility to Evaluate Scientific LiteratureKnowledge of Treatment ParadigmsExperience in Field Medical RolesAbility to Communicate Complex DataKnowledge of Healthcare SystemsExperience in Analytics Tools

Soft Skills

Relationship BuildingCollaboration SkillsProblem-Solving SkillsInfluencing StakeholdersHigh Level of Professionalism

Tools & Technologies

CRM SystemsDigital Engagement PlatformsCommunication ToolsAnalytics Tools

Certifications & Qualifications

Valid Driver’s License

Industry Keywords

Healthcare ProfessionalsClinical InsightsPatient CarePharmacovigilanceMedical StrategyResearch SitesInvestigator RelationshipsEquitable Access to Clinical Trials

About the role

Key responsibilities & impact

Engage in peer-to-peer scientific dialogue with Regional Thought Leaders, National Thought Leaders, and Healthcare Professionals within an assigned geography
Translate scientific data into clinical insights to support patient care and safe, effective use of BMS therapies
Serve as a clinical and scientific advisor to cross-functional partners
Provide field-based medical insights and support pre- and peri-launch activities aligned to medical strategy
Develop and maintain trusted relationships with academic and community Thought Leaders
Engage in proactive and reactive scientific dialogue to inform medical strategy and support product lifecycle management
Deliver educational presentations and scientific updates in individual and group settings, in-person and virtually
Collaborate with medical societies, patient advocacy groups, and guideline committees
Provide training and support for external speakers
Support payer engagement alongside cross-functional partners
Address unsolicited medical inquiries, including off-label questions, through Medical on Call engagements
Utilize digital tools and platforms to enhance engagement
Capture and document field insights and achieve defined annual goals
Advise clinical development teams on study and site feasibility
Maintain investigator relationships and support clinical trial awareness and participation
Identify and assess potential research sites for interventional and non-interventional studies
Support investigator-sponsored research processes and follow-up activities
Lead and support clinical evidence communications, including major data readouts
Ensure compliance with pharmacovigilance requirements, including adverse-event reporting
Collaborate with Global Development Operations and home office medical teams
Serve as a scientific expert and advisor to internal stakeholders
Partner across Medical, HEOR, and Commercial teams to align strategy
Support equitable access to clinical trials across healthcare systems
Represent BMS with integrity and compliance in external interactions
Maintain significant field presence and travel to engage healthcare professionals and stakeholders

Requirements

What you’ll need

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
Knowledge of scientific publications and data interpretation
Knowledge of pharmaceutical compliance and regulatory requirements
Knowledge of healthcare systems and patient access dynamics
Ability to communicate complex scientific data clearly and effectively
Strong understanding of clinical practice, treatment paradigms, and competitive landscape
Ability to critically evaluate scientific literature and clinical data
Understanding of patient journey and unmet needs
Demonstrated ability to build relationships and influence stakeholders
Strong collaboration and problem-solving skills in a matrix environment
Ability to analyze data and derive actionable insights
Experience using analytics tools such as CRM systems, CE³ or similar platforms
Ability to tailor engagement strategies based on HCP segmentation
Proficiency in digital engagement platforms and communication tools
Experience managing and tracking HCP interactions in CRM systems
Ability to work both independently and as part of a team
High level of professionalism, integrity, and compliance
Minimum age of 21
Valid driver’s license in good standing
Acceptable driving record
Must meet requirements to operate a company-provided vehicle

Benefits

Comp & perks

Comprehensive benefit plans including wellbeing support, retirement and financial protection benefits, and medical, dental, vision, life and disability insurance
Flexible Time Off (FTO) without a set accrual limit for eligible U.S.-based exempt employees
11 paid company holidays each year
160 hours of paid vacation annually for eligible new hires
3 optional holidays for eligible employees
Paid sick leave
Up to two paid volunteer days per year
Summer hours flexibility
Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees
Additional discretionary incentive cash and stock opportunities
Workplace accommodations/adjustments and ongoing support for people with disabilities