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Bristol Myers Squibb

Medical Science Liaison, Oncology, Lung & GU Tumors (Central & North Texas)

Bristol Myers Squibb, Dallas, Texas, United States, 75215

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Medical Science Liaison, Oncology, Lung & GU Tumors (Central & North Texas) – Bristol Myers Squibb

While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required. Location: Central & North Texas / Oklahoma Overview The Medical Science Liaison (MSL) engages in meaningful peer-to-peer scientific dialogue with healthcare system leaders and top HCPs within a defined geography to translate science into patient care. The MSL captures medical insights and acts as a clinical and scientific advisor to cross-functional partners, ensuring interactions align with enterprise and medical strategies to support patient access to BMS medicines. Key Responsibilities

Develop trusted relationships with academic and community Thought Leaders in Oncology through high-quality peer-to-peer scientific dialogue in proactive and reactive settings (1:1, group presentations, virtual, etc.). Engage with TLs to gain insights on the clinical landscape and develop a medical plan aligned with product and disease area goals, supporting launch and lifecycle activities. Engage medical societies, patient advocacy groups, and guideline committee members as appropriate. Provide training for external speakers as needed. Strategically engage payers in pre- and peri-launch phases (with HEOR and Account Executives). Provide medical support to address unsolicited HCP questions in real time, in person or via Medical on Call (virtual). Document and achieve annual goals; leverage digital capabilities to enhance medical engagement. Clinical Trial engagement: provide recommendations and insights to the clinical development team on study feasibilities based on field knowledge; liaise with large accounts to address clinical barriers to patient access and equity in access to trials; lead major evidence read-outs with investigators; support ISR submissions and execution; ensure pharmacovigilance practices are understood and followed by investigators; support CRO-sponsored studies when applicable. Qualifications & Experience

MD, PharmD, PhD, APP, PA, NP with disease-area expertise or relevant pharmaceutical experience; field medical or trial experience preferred. Strong oncology experience and deep understanding of TL environments and needs. Knowledge of scientific publications, clinical trial design, and national/regional healthcare and access environments. Travel

Role requires field-based work; majority of time in the field with external stakeholders and internal support as needed. Company-provided vehicle and driving requirements apply (age, license, driving risk). Key Competencies

Scientific agility, ability to discuss data clearly and credibly with TLs/HCPs; strong communication and presentation skills; continuous learning mindset. Patient centricity; customer-focused/enterprise mindset; problem-solving and relationship-building across matrix organizations. Analytical capability and ability to derive insights from data and analytics; proficiency with CE^3 and CRM tools. Technological agility and comfort with digital channels to engage HCPs and stakeholders. Teamwork and cross-functional collaboration; understanding of RWE and national access environments. Compensation & Benefits Field – United States – US $163,330 - $197,915. Additional incentive cash and stock opportunities may be available. Benefits include health, wellbeing, financial, paid time off, and other programs in alignment with applicable plans and location. Equal Opportunity BMS is committed to equal employment opportunity. Reasonable accommodations are available for applicants with disabilities. For inquiries, contact adastaffingsupport@bms.com. For more information, visit careers.bms.com/eeo-accessibility.

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