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Drug Safety Specialist/ Clinical Safety Coordinator (Nursing Professionals Encouraged To Apply)

Medpace
Medpace
1-4 years
preferred by company
10 Dec. 22, 2025
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

Drug Safety Specialist / Clinical Safety Coordinator

(Nursing Professionals Encouraged to Apply)

Location: Navi Mumbai, India
Employment Type: Full-Time, Office-Based
Functional Area: Clinical Safety / Pharmacovigilance
Industry: Pharmaceutical, Biotechnology & CRO
Experience Required: 1–4 Years (Clinical Safety / Pharmacovigilance / Clinical Research)


Job Overview

We are seeking a Drug Safety Specialist / Clinical Safety Coordinator to join a growing Clinical Safety team in India. This role is responsible for the end-to-end handling and processing of adverse events arising from clinical trials and post-marketing surveillance activities.

This opportunity is well suited for nursing professionals and healthcare graduates who are looking to transition into or further build a career in pharmacovigilance and clinical safety within a global clinical research environment.


Key Responsibilities

  • Determine appropriate action plans for incoming safety-related communications and calls

  • Collect, process, and track adverse events (AEs) and serious adverse events (SAEs) from all sources

  • Perform accurate and timely case processing in accordance with safety SOPs and regulatory timelines

  • Prepare clear, medically sound safety narratives

  • Generate and contribute to safety data reports and metrics

  • Collaborate with internal clinical teams and investigative research sites to ensure compliance with safety reporting processes

  • Support ongoing clinical trial safety oversight and post-marketing pharmacovigilance activities

  • Maintain accurate documentation and ensure audit-ready safety records


Required Qualifications

  • Bachelor’s degree in a healthcare-related field such as:

    • Nursing

    • Pharmacy

    • Pharmacology

    • Life Sciences or related disciplines

  • Clinical experience or experience in clinical research, pharmacovigilance, case processing, or post-marketing safety is preferred

  • Proficiency in spoken and written English

  • Strong working knowledge of Microsoft Office applications

  • Solid understanding of medical terminology

  • Excellent organizational, communication, and documentation skills

  • Ability to manage multiple tasks with attention to detail in a regulated environment


Why This Role

  • Ideal entry-to-mid-level opportunity for nurses and healthcare professionals moving into pharmacovigilance

  • Exposure to global clinical safety operations across Phase I–IV studies

  • Structured career development pathways within clinical safety and drug safety functions

  • Opportunity to work in a scientifically driven, patient-focused organization


About the Organization

Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With expertise across major therapeutic areas—including oncology, cardiology, CNS, metabolic disorders, and infectious diseases—Medpace operates in 40+ countries and employs over 5,000 professionals worldwide.


Employee Benefits & Growth

  • Flexible and supportive work environment

  • Competitive compensation and comprehensive benefits

  • Generous paid time off policies

  • Structured career progression and professional development programs

  • Employee wellness initiatives and engagement programs

  • Company-sponsored recognition and appreciation events


Awards & Recognition

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)

  • Multiple CRO Leadership Awards from Life Science Leader magazine for quality, expertise, and reliability


Disclaimer

This job description outlines the general scope of responsibilities and qualifications and is not intended to be an exhaustive list. Duties may evolve based on organizational and project requirements.