Medical Science Liaison / Senior Medical Science Liaison, Pumitamig, International Markets, India and Thailand

Working with UsChallenging. 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.Role SummaryThe Medical Science Liaison / Senior Medical Science Liaison (MSL) advances the BMS medical mission by building trusted, peer-to-peer scientific partnerships and delivering timely data and actionable insights that support appropriate use of BMS medicines and improve patient care.This is a field-based role. The MSL / Senior MSL is expected to spend approximately 80–90% of their time with external stakeholders (e.g., investigators and clinical thought leaders), while maintaining strong therapeutic-area expertise and supporting internal stakeholders. Field time may vary based on asset life cycle, therapeutic area, and geographic scope. Travel is required and will include international travel.The MSL / Senior MSL, Oncology, will act as the country field medical lead, engaging clinical investigators and TLs, serving as the therapeutic resource for external and internal stakeholders. A key differentiator of this senior role is a strong focus on clinical trial engagement, including leading investigator relationships, supporting site feasibility, enabling patient recruitment, and facilitating evidence-generation activities in close collaboration with Regional Clinical Operations (RCO). The MSL / Senior MSL also develops and executes a territory plan that supports medical education and disease-landscape shaping, aligned with the local Oncology Medical Affairs strategy. This role reports to the Regional Medical Market Lead.All activities are performed in an ethical and compliant manner, in full adherence with all applicable BMS policies, local laws, and external regulations.Key Responsibilities1. External Engagement and Customer FocusDevelop, maintain, and deepen trusted peer-to-peer relationships with National and Regional (above market) Thought Leaders (NTLs/RTLs), HCPs, patient advocacy groups (PAGs), medical societies, and payer stakeholders within a defined geographic scope.Engage with TLs/HCPs through multiple channels (e.g., 1:1 meetings, group presentations, virtual/remote interactions).Continuously profile and assess the medical landscape within the therapeutic area, maintaining up-to-date knowledge of treatment strategies, clinical trial activities, unmet medical needs, competitive landscape, and scientific developments.Effectively present scientific and clinical information to HCPs, ensuring medical accuracy and full compliance with local procedures, ethical guidelines, and legal and regulatory directives.Identify and engage potential speakers for BMS educational programmes, ensuring all speakers receive appropriate product and disease-state training.Engage strategically with payers during pre- and peri-launch phases in collaboration with Field HEOR and Account Executives where applicable.Support acceleration of pipeline impact and launch readiness through HCP engagement, medical education, advisory boards, and scientific exchange.Leverage digital tools and capabilities — including AI — to enhance the quality, reach, and efficiency of medical engagement.2. Clinical Trial Support and Evidence Generation Serve as the primary point of contact between clinical trial investigators and the BMS Medical/Global Development Operations (GDO) team, as aligned with local medical leadership.Support Interventional and Non-Interventional Research (NIR) studies by identifying and assessing potential study sites, facilitating patient recruitment, and supporting discussions around the safe and effective use of BMS investigational products — in accordance with local medical management direction and the relevant study scope document.Provide feasibility insights to the clinical development team (study and site), based on field knowledge and investigator relationships.Actively support CRO/RCO-sponsored studies as agreed with local medical management and as defined by the applicable study scope document.Support Investigator-Sponsored Research (ISR) and collaborative study submissions and execution processes, including follow-up, in accordance with BMS guidance.Liaise with key accounts to understand clinical barriers to patient access and promote equity in access to clinical trials.Lead or support investigator meetings, as agreed with local and regional medical management.Contribute to the involvement of TLs in local and/or GDO-driven studies, Managed Access Protocols (MAP), and other scientific activities.Ensure that BMS Pharmacovigilance procedural documents are understood and applied by all investigators in local studies; promptly alert appropriate BMS personnel to any identified Adverse Events (AEs).3. Medical Planning and ExecutionContribute to the Local/Regional Medical Plan (e.g., clinical trial support, ISR strategy, and medical-insight priorities).Develop and execute a Scientific engagement plan aligned with therapeutic area objectives and stakeholder needs.Use an institution/account planning approach and contribute to cross-functional institution and account plans.Contribute to medical strategy by sharing medical insights and disease-area knowledge, grounded in patient needs and treatment trends.