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Assoc Medical Safety Dir

0-2 years
Not Disclosed
10 Sept. 23, 2025
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

Associate Medical Safety Director

Location: Kolkata, India
Job ID: R1474799
Job Type: Full-time
Additional Locations: Available


Company Overview

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.

Learn more about IQVIA Careers


Job Overview

The Associate Medical Safety Director (AMSD) provides medical expertise in pharmacovigilance for assigned trials and stand-alone safety projects. The role involves medical review, oversight, and consultation under appropriate guidance from management or senior medical safety directors.


Essential Functions

Medical Review & Oversight

  • Review and clarify trial-related Adverse Events (AEs) and post-marketing Adverse Drug Reactions (ADRs), including narratives, coding, expectedness, seriousness, causality, and summaries.

  • Compose, edit, and medically review Analyses of Similar Events (AOSE) as per regulatory requirements.

  • Conduct aggregate reviews of safety information, including clinical data, to monitor a product’s safety profile.

  • Review and provide medical oversight on protocols, Investigational Drug Brochures (IDB), and Case Report Forms (CRFs) for safety content and data capture.

  • Provide medical review for IND Annual Reports, EU Periodic Reports, Development Risk Management Plans, Risk Evaluation and Mitigation Strategies (REMS), and safety-related submissions.

Advisory & Consultation

  • Serve as an internal consultant to pharmacovigilance case processing teams.

  • Provide medical oversight for label development and review.

  • Attend and contribute to Data Safety Monitoring Boards (DSMBs) and Safety Monitoring Committees.

  • Act as Global Safety Physician, assistant, or backup on assigned projects.

  • Provide medical escalation support for regulatory or project-related issues.

Communication & Collaboration

  • Represent safety and clinical data review findings in client and project meetings.

  • Maintain coverage for all medical safety deliverables within regulatory or contracted timelines.

  • Stay informed of industry developments in medical safety and pharmacovigilance.


Qualifications

Education & Experience

  • Medical degree from an accredited, internationally recognized medical school (Required).

  • 3 years clinical practice experience plus 2 years in the pharmaceutical or associated industry, or equivalent combination of education, training, and experience (Required).

  • Valid medical license or equivalent in country/region of work (Preferred).

Knowledge & Skills

  • Knowledge of federal/local regulations and guidelines for clinical research, safety, and good clinical practice.

  • Familiarity with clinical trials and pharmaceutical research processes.

  • Ability to prioritize, meet deadlines, and provide consultation across multiple assignments.

  • Excellent initiative, flexibility, and interpersonal skills.

  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.


Application

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