Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Director, Medical Safety Assessment Physician

Bristol Myers Squibb
Bristol Myers Squibb
3+ years
Not Disclosed
Hyderabad, India
10 Feb. 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Director – Medical Safety Assessment Physician
Location: Hyderabad, Telangana, India
Job Requisition ID: R1599165
Company: Bristol Myers Squibb (BMS)
Function: Pharmacovigilance / Global Patient Safety
Employment Type: Full-Time

ThePharmaDaily.com is featuring a senior leadership opportunity for an experienced Medical Safety Physician to join global pharmacovigilance operations as Director – Medical Safety Assessment Physician. This strategic role is responsible for leading benefit-risk strategy, safety governance, signal management, and regulatory safety oversight across development and marketed products.

This position is ideal for senior pharmacovigilance leaders with strong clinical expertise and global regulatory experience in drug safety lifecycle management.

Role Overview

The Director, Medical Safety Assessment Physician will lead product safety strategy for assigned compounds across development and post-marketing phases. The role includes chairing Safety Management Teams (SMTs), overseeing aggregate safety reporting, leading safety signal evaluation, supporting regulatory labeling activities, and representing Patient Safety (PS) at Health Authority and Data Monitoring Committee meetings.

This is a high-impact leadership role within global R&D and pharmacovigilance operations.

Key Responsibilities

Global Product Safety Leadership

  • Lead safety strategy and benefit-risk management for assigned compounds.

  • Chair Safety Management Teams (SMTs).

  • Oversee preparation and review of aggregate safety reports including:

    • Development Safety Update Reports (DSUR)

    • Periodic Benefit-Risk Evaluation Reports (PBRER)

  • Review safety sections of regulatory and clinical documents including:

    • Protocols, Investigator Brochures (IB), Clinical Study Reports (CSR)

    • Clinical Trial Applications (CTA) and Marketing Authorization Applications (MAA)

Safety Signal Management

  • Lead evaluation and management of safety signals from multiple data sources including case series, literature, claims databases, and Health Authority communications.

  • Develop and document signal evaluation strategies via Safety Topic Reviews and Signal Reports.

  • Drive safety-focused risk mitigation strategies across product lifecycle.

Clinical Development Safety Oversight

  • Act as Global Safety Lead for compounds in development.

  • Provide safety input to clinical development plans, protocols, SAPs, ICFs, and CSRs.

  • Lead development of safety risk language and risk management strategies.

  • Support integrated safety summaries and regulatory submission documents.

  • Represent Patient Safety in pre-submission, Scientific Advice, Advisory Committee, and DMC meetings.

Post-Marketing Safety Management

  • Serve as safety lead for marketed products.

  • Ensure emerging safety data is reflected in global labeling updates.

  • Lead post-marketing safety submissions and aggregate reporting.

  • Provide oversight of risk management plans (RMPs) and safety commitments.

  • Support responses to regulatory authority queries.

Regulatory & Inspection Readiness

  • Support EU Qualified Person for Pharmacovigilance (QPPV) and regional PV representatives.

  • Prepare for regulatory inspections and ensure alignment with global safety regulations.

  • Contribute to crisis management and safety issue escalation.

Cross-Functional & Strategic Contributions

  • Provide safety input into publication strategies and scientific communications.

  • Deliver internal safety training.

  • Act as liaison between Patient Safety and Legal, Manufacturing, Business Development, Medical Affairs, and Commercial teams.

  • Lead process improvement initiatives within Pharmacovigilance systems and procedures.

Experience Required

  • Minimum 3+ years of experience in Pharmacovigilance or relevant pharmaceutical/biomedical roles (Medical, Clinical Development, Regulatory Affairs).

  • Strong experience in global safety assessment, signal management, and regulatory submissions.

  • Prior leadership experience in safety strategy or product safety governance strongly preferred.

  • Experience across development and post-marketing safety phases desirable.

Educational Qualification

  • MD or equivalent medical degree (mandatory).

  • Postgraduate qualification or clinical experience in Internal Medicine, Oncology, Immunology, or related specialties preferred.

  • Experience in clinical research, observational research, or medical practice considered an advantage.

Core Competencies & Technical Expertise

  • In-depth understanding of the drug development lifecycle.

  • Strong knowledge of global pharmacovigilance regulations and safety reporting requirements.

  • Expertise in benefit-risk assessment and signal detection methodologies.

  • Experience preparing DSURs, PBRERs, integrated safety summaries, and regulatory safety documentation.

  • Proficiency in safety data evaluation using observational research methodologies.

  • Strong analytical reasoning and scientific judgment.

  • Ability to manage multiple global projects in a complex matrix organization.

  • Excellent verbal and written communication skills.

  • High attention to detail and regulatory compliance mindset.

Work Model

Role classification may include site-essential, hybrid (site-by-design), field-based, or remote-by-design structures depending on business needs. Onsite collaboration may be required as part of essential job responsibilities.

Why This Role Is Strategic

This leadership position directly influences global patient safety strategy, regulatory compliance, and product differentiation through evidence-based benefit-risk evaluation. It provides the opportunity to shape pharmacovigilance excellence within a global R&D ecosystem while impacting patient lives worldwide.

Explore more Pharmacovigilance, Drug Safety, Medical Affairs, and Global Regulatory leadership roles on ThePharmaDaily.com – your trusted global pharmaceutical career platform.