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Drug Safety Specialist/ Clinical Safety Coordinator

0-2 years
Not Disclosed
10 Oct. 30, 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

Position: Drug Safety Specialist / Clinical Safety Coordinator

Location: Navi Mumbai, India
Department: Clinical Safety
Job ID: 10603
Employment Type: Full-Time (Office-Based)


Job Summary

Medpace is seeking a Clinical Safety Coordinator to join our Clinical Safety department in India.
This role involves managing and processing adverse events (AEs) and serious adverse events (SAEs) from multiple sources, including clinical trials and post-marketing surveillance.

If you’re looking to apply your healthcare background in a growing global CRO and advance your career in Pharmacovigilance and Drug Safety, this is the ideal opportunity.


Key Responsibilities

  • Handle and process incoming adverse events and serious adverse events.

  • Determine appropriate actions for incoming safety reports and calls.

  • Write and review safety narratives for clinical and post-marketing cases.

  • Collect, process, and track safety data using internal systems.

  • Prepare and report safety data summaries for internal and regulatory purposes.

  • Collaborate with internal teams and clinical research sites to ensure safety process compliance.


Qualifications

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

  • Experience:

    • Clinical experience or exposure to Clinical Research, Case Processing, or Post-Marketing Pharmacovigilance preferred.

  • Skills:

    • Proficient in English (written and verbal).

    • Working knowledge of Microsoft Office (Word, Excel, Outlook).

    • Strong grasp of medical terminology.

    • Excellent organizational and communication skills.


About Medpace

Medpace is a full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
We aim to accelerate the development of safe and effective therapeutics through a scientific and disciplined approach, leveraging global regulatory and therapeutic expertise in major therapeutic areas including:

  • Oncology

  • Cardiology

  • Metabolic and Endocrine Disorders

  • CNS

  • Anti-Viral and Anti-Infective Studies

Headquarters: Cincinnati, Ohio
Global Presence: 40+ countries
Employees: 5,000+


Why Join Medpace?

People. Purpose. Passion. Make a Difference Tomorrow — Join Us Today.

Medpace Offers:

  • Flexible work environment

  • Competitive compensation & benefits

  • Generous PTO package

  • Structured career development & professional growth opportunities

  • Company-sponsored employee appreciation events

  • Health & wellness initiatives


Awards & Recognition

  • Forbes: America’s Most Successful Midsize Companies (2021–2024)

  • Life Science Leader: CRO Leadership Awards (Expertise, Quality, Reliability, and Compatibility)


Next Steps

A Medpace recruiter will review your qualifications.
If shortlisted, you will be contacted with details regarding the next steps in the recruitment process.

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