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

Bristol Myers Squibb
2-3 years
Not Disclosed
Remote, India, India
10 June 9, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Science Liaison / Senior Medical Science Liaison – Pumitamig (Oncology, International Markets: India & Thailand)
Job ID: R1603152
Company:
Bristol Myers Squibb
Location: Field-based – India (International coverage: India & Thailand)
Employment Type: Full-Time
Therapeutic Area: Oncology
Reporting Line: Regional Medical Market Lead


Role Summary

The Medical Science Liaison (MSL) / Senior MSL supports Bristol Myers Squibb’s medical mission by building strong scientific partnerships with healthcare professionals (HCPs), investigators, and key opinion leaders (KOLs). The role focuses on scientific exchange, clinical trial support, evidence generation, and medical insights collection to improve patient outcomes and support oncology product strategy.

This is a highly field-based role, with 80–90% external engagement and includes significant travel, including international travel across India and Thailand.


Key Responsibilities

External Scientific Engagement

  • Build and maintain peer-to-peer relationships with KOLs, investigators, HCPs, medical societies, payer stakeholders, and patient advocacy groups.

  • Deliver accurate, non-promotional scientific and clinical information across multiple channels (face-to-face, virtual, group presentations).

  • Maintain deep knowledge of oncology landscape including treatments, clinical trials, unmet needs, and competitive environment.

  • Identify and engage potential speakers for medical education programs.

  • Support advisory boards, scientific exchange meetings, symposia, and educational initiatives.

  • Support payer discussions during pre- and peri-launch phases (with HEOR and account teams).

  • Use digital tools and AI-enabled platforms to enhance engagement and insight generation.


Clinical Trial & Evidence Generation Support

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

  • Support interventional and non-interventional studies, including:

    • Site identification and feasibility assessment

    • Patient recruitment support

    • Investigator engagement

  • Support investigator-sponsored research (ISR) submissions and collaborative studies.

  • Provide real-world feasibility insights to clinical development teams.

  • Support CRO/RCO-sponsored studies and managed access programs.

  • Facilitate investigator meetings and study-related scientific discussions.

  • Ensure pharmacovigilance compliance and reporting of adverse events from the field.


Medical Planning & Execution

  • Contribute to local and regional medical plans and scientific engagement strategies.

  • Develop territory-level scientific engagement plans aligned with oncology strategy.

  • Provide insights from field interactions to inform medical strategy and portfolio decisions.

  • Support cross-functional account planning and institutional engagement strategies.

  • Contribute to pricing and reimbursement scientific documentation where applicable.


Medical Insights & Intelligence Gathering

  • Collect and communicate actionable medical insights from the field.

  • Monitor treatment trends, competitive intelligence, and evolving clinical practices.

  • Share insights with internal stakeholders to support strategy and decision-making.

  • Maintain accurate documentation of field activities and insights.


Internal Scientific Support

  • Deliver scientific presentations at internal and external medical meetings.

  • Support training of internal teams including:

    • Commercial

    • Clinical Operations (RCO)

    • Regulatory Affairs

    • Pharmacovigilance

    • Market Access

    • HEOR

  • Provide product and disease-area training to clinical trial site staff.


Compliance & Ethics

  • Ensure all activities comply with:

    • Internal BMS policies

    • Local regulations

    • Global healthcare compliance standards

  • Maintain ethical, transparent, and non-promotional scientific communication.

  • Report adverse events promptly to pharmacovigilance teams.

  • Act as a compliance role model in all external and internal interactions.


Minimum Requirements

Education

  • Advanced scientific or medical degree: MD, PharmD, or PhD (Oncology or related field preferred)

  • Alternatively, a Science graduate with strong pharmaceutical/industry experience

Experience

  • 2–3+ years of MSL experience preferred

  • Minimum 2 years in customer-facing pharmaceutical/clinical role

  • Oncology clinical or scientific research experience required

  • Strong exposure to clinical trials, investigator engagement, and ISR processes


Core Skills & Competencies

Scientific & Clinical Skills

  • Oncology therapeutic knowledge

  • Clinical trial design and execution understanding

  • Evidence generation (ISR, RWE, NIS studies)

  • Data interpretation and scientific communication

Engagement & Relationship Skills

  • KOL relationship management

  • Stakeholder engagement

  • Scientific dialogue and education delivery

  • Cross-functional collaboration

Strategic & Analytical Skills

  • Medical insight generation

  • Competitive intelligence analysis

  • Strategic territory planning

  • Evidence-based decision-making

Digital & Professional Skills

  • Digital engagement tools usage

  • AI-enabled scientific communication tools

  • Presentation and communication skills

  • Data documentation and reporting


Ideal Candidate Profile

  • Strong oncology background with clinical research exposure

  • Experienced in field medical roles or clinical stakeholder engagement

  • Skilled in translating complex scientific data into practical clinical insights

  • Comfortable working in a highly field-based, travel-intensive role

  • Strong ethical grounding and compliance-first mindset

  • Ability to influence without promotion, through science-driven engagement