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Bristol Myers Squibb

Medical Science Liaison, Neurodegeneration

Bristol Myers Squibb

. Engage in peer-to-peer scientific dialogue with regional, national, and healthcare professional thought leaders within a defined geography .

Posted 9/30/2026full-timeAnn Arbor • Michigan • United StatesMid-LevelSenior💰 $166,090 - $201,262 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in engaging healthcare professionals and thought leaders, translating scientific evidence into patient care, and navigating the pharmaceutical industry. Proficient in clinical trial design, regulatory compliance, and leveraging data analytics to inform medical strategies.

Highest-signal resume keywords
MD, PharmD, PhD, APP, PA, NPNeurology ExperienceClinical Trial DesignGood Clinical PracticesRWE Interpretation

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Scientific Disease-Area KnowledgePatient Treatment TrendsClinical Landscape KnowledgeData AnalysisMedical Engagement
Soft Skills
Excellent Communication SkillsRelationship BuildingProblem SolvingInfluencing SkillsTeam Collaboration
Tools & Technologies
CE^3 Analytics EngineMedical on Call TechnologyCRM Tools
Industry Keywords
Pharmaceutical IndustryCompliance GuidelinesRegulatory RequirementsHealthcare Delivery ModelsTreatment Paradigms

About the role

Key responsibilities & impact
  • Engage in peer-to-peer scientific dialogue with regional, national, and healthcare professional thought leaders within a defined geography
  • Engage top HCPs in high-disease-burden hospitals
  • Translate scientific evidence into patient care
  • Capture medical insights and advise cross-functional partners as a clinical and scientific advisor
  • Ensure interactions align with enterprise and medical strategies and support patient access to BMS medicines
  • Address scientific questions beyond approved assets and indications
  • Conduct pre-launch, peri-launch, and lifecycle medical engagement
  • Deliver educational dialogue and share clinical evidence according to physician needs and the field medical plan
  • Serve on a scheduled basis as Medical on Call, answering unsolicited off-label and technically complex questions virtually
  • Spend the majority of time in the field interacting with investigators, clinical thought leaders, and other external stakeholders
  • Develop trusted relationships with academic and community neurology thought leaders through proactive and reactive interactions
  • Collaborate with thought leaders to gather clinical-landscape insights and develop product- and disease-focused medical plans
  • Engage medical societies, patient advocacy groups, and guideline committee members
  • Train external speakers as needed
  • Engage payers during pre- and peri-launch phases with fHEOR and Account Executives
  • Document and achieve annual goals
  • Leverage digital capabilities to enhance medical engagement
  • Advise clinical development teams on study and site feasibility
  • Liaise with large accounts regarding clinical barriers and equitable access to trials
  • Lead major evidence read-outs with clinical trial investigators
  • Support interventional and non-interventional research studies, including identifying and assessing study sites
  • Support HCPs through ISR submission, execution, and follow-up
  • Ensure investigators understand and apply BMS pharmacovigilance procedures and alert personnel to adverse events
  • Support CRO-sponsored studies as agreed with home office medical and GDO

Requirements

What you’ll need
  • MD, PharmD, PhD, APP, PA, or NP with experience in a specific disease area, broad medical background, or relevant pharmaceutical experience
  • Experience working in a scientific and/or clinical research environment
  • Field medical expertise preferred
  • Deep understanding of the Thought Leader environment and needs
  • Strong neurology experience required
  • Scientific or clinical disease-area knowledge, patient treatment trends, and clinical landscape knowledge
  • Knowledge of the pharmaceutical industry, including compliance and regulatory guidelines
  • Understanding of scientific publications
  • Knowledge of clinical trial design and process
  • Understanding of national and regional healthcare and access environments
  • Ability to engage in compelling, fair, and balanced scientific dialogue about data
  • Expert knowledge of clinical practice and evolving healthcare delivery models
  • Ability to critically appraise scientific publications
  • Knowledge of Good Clinical Practices and ethical, governmental, and regulatory requirements
  • Understanding of treatment paradigms and competitive landscape
  • Excellent communication and presentation skills
  • Experience identifying, engaging, and cultivating relationships with HCPs
  • Ability to influence a matrix organization and solve problems
  • Ability to analyze market trends and HCP preferences
  • Ability to segment HCPs based on preferences and relevant factors
  • Ability to derive actionable insights from data and analytics, including CE^3 analytics engine
  • Competency using CE^3 and other software or CRM tools to manage HCP data and interactions
  • Ability to use Medical on Call technology
  • Ability to use internet and online resources effectively
  • Ability to work independently and as a team player with internal and external stakeholders
  • Deep knowledge and experience of RWE; ability to interpret RWE and identify RWE opportunities
  • High integrity and good judgment
  • Willingness to travel
  • Must live within the managed territory or within 50 miles of the territory borders
  • Must be at least 21 years old
  • Must hold a driver’s license in good standing issued by the state of residence
  • Must meet the Company’s acceptable driving-risk requirements

Benefits

Comp & perks
  • Additional discretionary incentive cash and stock opportunities
  • Wellbeing support
  • Retirement and financial protection benefits
  • Medical, dental, vision, life and disability insurance offerings
  • 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 non-exempt, RayzeBio, and Puerto Rico employees
  • Paid sick leave
  • Up to two paid volunteer days per year
  • Summer hours flexibility
  • Medical, personal, parental, caregiver, bereavement, or military leaves of absence
  • Annual Global Shutdown between Christmas Day and New Year's Day
  • Reasonable workplace accommodations/adjustments
  • Flexible work models, including field-based and remote-by-design arrangements