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

Bristol Myers Squibb
2+ years
INR 30 LPA – 60 LPA
PAN-India, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Medical Science Liaison / Senior Medical Science Liaison – Pumitamig, International Markets (India & Thailand)

Location: Field – India
Job ID: R1603152
Job Type: Full-Time

About the Company

Working at Bristol Myers Squibb means contributing to meaningful, challenging, and life-changing work. The organization is focused on advancing breakthrough therapies in areas such as oncology and cell therapy, transforming patient outcomes globally. Employees work in a high-performance, science-driven environment with strong emphasis on innovation, collaboration, and ethical integrity.


Role Summary

The Medical Science Liaison (MSL) / Senior MSL advances the medical mission by building trusted scientific partnerships with key external stakeholders and delivering actionable insights that support appropriate use of therapies.

This is a field-based, oncology-focused role, requiring approximately 80–90% external engagement with healthcare professionals, investigators, and thought leaders across India and Thailand, with international travel as required.

A key responsibility includes clinical trial engagement, investigator support, and evidence generation activities in collaboration with clinical operations teams.


Key Responsibilities

External Scientific Engagement

  • Build and maintain strong peer-to-peer relationships with key opinion leaders (KOLs), investigators, HCPs, medical societies, and patient advocacy groups.

  • Deliver accurate, compliant scientific and clinical information through 1:1 and group engagements.

  • Continuously monitor and analyze therapeutic landscape, unmet needs, and competitive developments.

  • Support medical education, advisory boards, and scientific exchange programs.

  • Identify and support speaker development for educational initiatives.


Clinical Trial & Research Support

  • Act as a key scientific liaison between investigators and clinical development teams.

  • Support site identification, feasibility assessments, and patient recruitment.

  • Facilitate Interventional and Non-Interventional Research activities.

  • Support Investigator-Sponsored Research (ISR) submissions and collaborations.

  • Assist investigator meetings and site engagement activities.

  • Ensure proper pharmacovigilance awareness and adverse event reporting from sites.


Medical Strategy & Planning

  • Contribute to local and regional medical planning activities.

  • Develop and execute scientific engagement and territory plans.

  • Support advisory boards, symposia, and expert meetings.

  • Provide scientific input for pricing, reimbursement, and access strategies where applicable.


Medical Insights & Intelligence

  • Capture and communicate field insights to internal stakeholders.

  • Provide competitive intelligence and treatment landscape updates.

  • Document all scientific interactions and ensure alignment with business objectives.

  • Support data-driven decision-making across medical and commercial functions.


Internal Collaboration & Support

  • Provide scientific training and updates to internal teams including Medical Affairs, Clinical Operations, Regulatory, HEOR, Market Access, and Pharmacovigilance.

  • Support internal scientific meetings and speaker evaluations.

  • Ensure alignment between field activities and global medical strategy.


Compliance & Ethics

  • Adhere strictly to company policies, ethical guidelines, and regulatory requirements.

  • Ensure compliant scientific communication and interactions.

  • Report adverse events and safety information in coordination with Pharmacovigilance teams.

  • Act as a role model for integrity and ethical behavior in all field activities.


Required Qualifications

Education

  • Advanced degree required: MD / PharmD / PhD (preferably in Oncology or related field)

  • Alternatively, a Life Sciences graduate with strong relevant pharmaceutical/industry experience.

Experience

  • Minimum 2–3 years of MSL experience preferred.

  • At least 2+ years in a customer-facing pharmaceutical or clinical research role.

  • Strong background in oncology and clinical research environments.

  • Experience in clinical trial support including site engagement and patient recruitment.

  • Experience working with KOLs and healthcare professionals.