If you’re a fresh nursing graduate looking to enter pharmacovigilance, this Clinical Safety Coordinator job in Navi Mumbai offers a strong career start in drug safety and clinical research. This opportunity is ideal for candidates aiming to build expertise in adverse event reporting, safety data processing, and clinical safety operations.
This role provides hands-on exposure to clinical trials and post-marketing surveillance (PMS) within a globally recognized CRO, making it a valuable entry point into the pharmacovigilance (PV) industry.
Job Overview
- Role: Clinical Safety Coordinator (Entry-Level)
- Location: Navi Mumbai, India
- Department: Clinical Safety / Pharmacovigilance
- Experience: Freshers (Nursing Graduates)
- Employment Type: Full-Time
Key Responsibilities
As a Clinical Safety Coordinator, you will:
- Handle incoming adverse event (AE) and serious adverse event (SAE) reports
- Determine appropriate action plans for safety-related calls
- Collect, process, and track safety data from multiple sources
- Prepare and write safety narratives
- Generate reports on clinical safety data
- Collaborate with internal teams and clinical research sites
- Ensure compliance with global pharmacovigilance guidelines and safety processes
Eligibility Criteria
To apply for this entry-level pharmacovigilance job, candidates must have:
- Bachelor of Science in Nursing (BSc Nursing) or higher (MSc preferred)
- Clinical experience in a hospital or healthcare setting
- Good knowledge of medical terminology
- Proficiency in Microsoft Office tools
- Strong communication and organizational skills
Why Start Your PV Career Here?
This role is highly suitable for candidates searching for:
- Pharmacovigilance jobs for freshers in India
- Clinical safety jobs after BSc Nursing
- Entry-level drug safety associate roles
- CRO jobs in Navi Mumbai for nurses
You will gain structured training in drug safety case processing, a critical skill in the global pharmaceutical industry.
Salary & Benefits
- Estimated Salary: โน3,00,000 โ โน5,00,000 per annum
- Flexible work environment
- Competitive compensation and PTO
- Structured career growth in pharmacovigilance
- Employee wellness programs
- Recognition and reward programs
About the Company
Medpace is a global Contract Research Organization (CRO) providing Phase IโIV clinical development services across therapeutic areas such as oncology, cardiology, CNS, and infectious diseases. With operations in 40+ countries, it is known for its scientific rigor and regulatory expertise.
How to Apply
