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Drug Safety Specialist/ Clinical Safety Coordinator

2+ years
₹4 – ₹6 LPA
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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
Location: Navi Mumbai, India

Job Description:
Medpace is hiring a Clinical Safety Coordinator / Drug Safety Specialist to support its expanding Clinical Safety department. This full-time, office-based position is ideal for professionals passionate about pharmacovigilance, clinical safety, and drug development. The selected candidate will be responsible for processing adverse events from clinical trials and post-marketing surveillance while ensuring regulatory compliance and data integrity.

Key Responsibilities:

  • Determine and execute action plans for incoming safety-related calls.

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

  • Write safety narratives for adverse events in alignment with clinical study timelines and regulatory expectations.

  • Analyze and report on safety data, supporting regulatory submissions and internal safety reviews.

  • Collaborate with internal departments and research sites to ensure compliance with global safety reporting standards.

Qualifications:

  • Bachelor’s degree in a healthcare-related field (Nursing, Pharmacy, Pharmacology, etc.).

  • Prior experience in clinical research, case processing, or post-marketing pharmacovigilance is preferred.

  • Proficient in English communication, both written and verbal.

  • Familiarity with Microsoft Office Suite.

  • Strong understanding of medical terminology.

  • Excellent organizational and communication skills.

Why Join Medpace?

  • Flexible work environment

  • Competitive compensation and benefits package

  • Generous PTO and leave policies

  • Defined career development pathways

  • Health and wellness initiatives

  • Regular employee appreciation events

About Medpace:
Medpace is a global clinical contract research organization (CRO) providing comprehensive Phase I–IV development services. Headquartered in Cincinnati, Ohio, and operating in 40+ countries with over 5,000 employees, we specialize in a wide range of therapeutic areas including oncology, cardiology, CNS, metabolic disorders, and infectious diseases.

Awards and Recognition:

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

  • Honored with multiple CRO Leadership Awards for performance in quality, capabilities, and reliability

Estimated Salary: ₹4 – ₹6 LPA (based on role expectations and experience)