Healthcare Job: Drug Safety Specialist at Medpace Mumbai
If you’re seeking a rewarding healthcare job that combines clinical expertise with global impact, the Drug Safety Specialist position at Medpace offers an exceptional opportunity. Located in Navi Mumbai, this role is ideal for professionals exploring jobs in Mumbai and those eager to grow within Medpace careers, with hands-on involvement in clinical safety and pharmacovigilance processes.
Job Details:
- Job Position: Drug Safety Specialist / Clinical Safety Coordinator
- Location: Navi Mumbai, India
- Department: Clinical Safety
- Job ID: 10603
About the Company
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I–IV clinical development services for biotechnology, pharmaceutical, and medical device industries. Its mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas, Medpace continues to be a leading employer for professionals searching for Medpace careers and stable jobs in Mumbai within the clinical research domain.
Healthcare Job – Qualifications
- Bachelor’s degree in healthcare-related field
- Clinical experience or Clinical Research, case processing and Post marketing Pharmacovigilance experience is preferred;
- Proficient English is required
- Proficient knowledge of Microsoft® Office;
- Broad knowledge of medical terminology; and
- Strong organizational and communication skills.
Job Description
This Drug Safety Specialist / Clinical Safety Coordinator role is designed for individuals passionate about clinical safety and healthcare operations. The role provides exposure to adverse event processing, safety data reporting, and cross-functional clinical research collaboration – making it a strong fit for anyone seeking a growth-oriented healthcare job.
Healthcare Job – Key Responsibilities
- Determine plan of action for incoming calls;
- Collect, process, and track incoming adverse and serious adverse events;
- Write safety narratives;
- Report on various safety data; and
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
