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Medpace Drug Safety Specialist Jobs 2026 | Clinical Safety Coordinator Vacancy in Navi Mumbai
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Medpace Drug Safety Specialist Jobs 2026 | Clinical Safety Coordinator Vacancy
(Medpace Drug Safety Specialist Jobs 2026)
🧾 Introduction
If you are a nursing or life sciences professional looking to enter the fast-growing field of pharmacovigilance and clinical research, then this opportunity is highly valuable. Medpace, a global CRO leader, is hiring Drug Safety Specialists and Clinical Safety Coordinators in Navi Mumbai. This role provides hands-on exposure to adverse event processing, ICSR documentation, and global drug safety operations, making it ideal for candidates aiming for a long-term career in pharmacovigilance.
🏢 About The Company – Medpace
Medpace is a globally recognized Contract Research Organization (CRO) that provides full-service clinical research solutions to pharmaceutical, biotechnology, and medical device companies.
Headquarters: Cincinnati, Ohio, USA
Founded: 1992
Industry: Clinical Research / CRO
Employees: 5,000+ globally
Global Presence: 40+ countries
The company is known for conducting Phase I–IV clinical trials and supporting drug development across multiple therapeutic areas such as oncology, cardiology, CNS, and infectious diseases.
📊 Job Overview Summary
This role focuses on drug safety and clinical safety operations, where candidates will manage adverse event reporting, case processing, and regulatory compliance. It is a perfect entry point for professionals transitioning into pharmacovigilance or CRO-based clinical research careers.
📌 Vacancy Details
Position: Drug Safety Specialist / Clinical Safety Coordinator
Company: Medpace
Location: Navi Mumbai, India
Experience: 1–3 Years
Qualification: Nursing (Mandatory)
Industry: Clinical Research / Pharmacovigilance
Employment Type: Full-Time
🔬 Responsibility Explanation
In this role, you will handle the complete lifecycle of drug safety data. Your primary responsibility will be to ensure that adverse events are properly documented, evaluated, and reported according to global pharmacovigilance standards.
You will work on processing safety cases, writing narratives, and maintaining accurate safety databases. Additionally, you will coordinate with clinical teams and ensure compliance with regulatory guidelines, which is critical for patient safety and successful clinical trials.
🎓 Eligibility Criteria
Nursing degree (Mandatory)
Strong understanding of medical terminology
Basic knowledge of pharmacovigilance and drug safety
Good communication skills (English)
MS Office proficiency
🧠 Skills Required
To succeed in this pharmacovigilance job, candidates should develop:
Knowledge of ICSR processing and adverse event reporting
Understanding of GCP and pharmacovigilance guidelines
Strong analytical and documentation skills
Attention to detail in safety case processing
Communication and coordination abilities
Time management and multitasking skills
💰 Salary Estimate
The estimated salary for this role ranges between ₹4.5 LPA and ₹8 LP, depending on experience and skill level.
Candidates entering pharmacovigilance can expect steady salary growth as they gain experience in drug safety, regulatory reporting, and clinical research operations.
1. Can freshers apply for Medpace drug safety jobs?
Freshers are not preferred, but candidates with basic pharmacovigilance knowledge or a healthcare background may be considered.
2. Is nursing mandatory for this role?
Yes, this specific role requires a nursing qualification.
3. What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report, which is used to document adverse drug reactions.
4. What career growth is available in pharmacovigilance?
You can grow into roles like Drug Safety Associate, Safety Scientist, and PV Manager.
5. Is this a good career option?
Yes, pharmacovigilance offers global opportunities, job stability, and strong salary growth.
🧾 Final Conclusion
The Medpace Drug Safety Specialist role is a golden opportunity for nursing professionals who want to transition into pharmacovigilance and clinical research. With structured training, global exposure, and hands-on experience in safety case processing, this job can serve as a strong foundation for a successful career in the pharmaceutical industry.
If you are serious about entering the drug safety domain, this is the right time to apply and build your expertise in pharmacovigilance operations.
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