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Manager, Drug Safety Physician, Pharmacovigilance Epidemiology & Risk Management

Cencora
Cencora
3+ years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Manager – Drug Safety Physician, Pharmacovigilance, Epidemiology & Risk Management

Location: Noida, India
Category: Consulting / Pharmacovigilance
Job Type: Full-Time
Experience Required: Minimum 3 Years
Job ID: R257963


About Cencora

Cencora is a global leader in pharmacovigilance, drug safety, and clinical risk management, committed to delivering innovative solutions that enhance patient safety. Our teams work across therapeutic areas to monitor, evaluate, and manage safety data, supporting healthcare providers, regulatory compliance, and improved patient outcomes.

Join Cencora to make a meaningful impact in drug safety, signal detection, and pharmacovigilance operations.


Position Overview

The Manager – Drug Safety Physician will conduct medical review and evaluation of Individual Case Safety Reports (ICSRs), oversee pharmacovigilance processes, and provide scientific input in risk management and signal detection activities. This role includes mentoring PV associates, collaborating with global PV teams, and ensuring adherence to regulatory guidelines and company SOPs.


Key Responsibilities

Medical Review & Case Assessment

  • Conduct medical review of ICSRs in the safety database, ensuring accurate classification of adverse events, seriousness criteria, MedDRA coding, suspect drugs, concomitant medications, lab data, medical history, and causality assessment.

  • Provide Company Clinical Comments and respond to queries from case owners.

  • Perform medical triage and scientific assessment of literature for safety-relevant publications.

  • Support periodic safety reporting including PSURs, PBRERs, and Risk Management Plans (RMPs).

Pharmacovigilance Oversight

  • Train and mentor PV associates on event capturing, safety data review, and pharmacovigilance best practices.

  • Maintain strong knowledge of GVP, GCP, ICH, EMA, and other regulatory guidelines.

  • Collaborate with Global Pharmacovigilance teams for signal detection and risk management initiatives.

  • Participate in internal and external audits/inspections to ensure compliance.

Communication & Collaboration

  • Maintain active communication with project teams and management regarding complex cases and safety concerns.

  • Actively participate in internal project meetings, providing scientific insights and operational support.

  • Escalate complex safety issues to Team Leads or Line Managers as appropriate.

Other Responsibilities

  • Perform any other drug safety and pharmacovigilance activities assigned by management.

  • Stay current with product safety profiles across multiple therapeutic areas.


Qualifications

  • Medical Degree (MBBS); PG degree in any discipline is advantageous but not mandatory.

  • Minimum 3 years of relevant experience in Pharmacovigilance & Drug Safety.


Skills & Competencies

  • Strong interpersonal and organizational skills; ability to work effectively in cross-functional teams.

  • High sense of responsibility, dedication, and ability to perform under pressure.

  • Strong scientific and clinical acumen for case evaluation and literature review.

  • Previous experience in corporate, pharmaceutical, or life sciences environments is advantageous.

  • Excellent English communication skills (written and verbal).


Why Join Cencora

  • Work with a global pharmacovigilance leader driving innovation in patient safety.

  • Gain exposure to clinical risk management, signal detection, and regulatory compliance.

  • Collaborate with cross-functional and global teams in a dynamic, professional environment.

  • Opportunities for career growth, professional development, and leadership in PV operations.


Equal Opportunity & Accessibility

Cencora is committed to diversity, equity, and inclusion, providing reasonable accommodations during the recruitment process consistent with legal requirements.

Apply today to advance your career in drug safety, pharmacovigilance, and risk management.