Medpace Drug Safety Specialist Jobs 2026 | Clinical Safety Coordinator Vacancy in Navi Mumbai

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.

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🏢 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.

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📊 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.

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📌 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

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🔬 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.

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🎓 Eligibility Criteria

• Nursing degree (Mandatory)
• Strong understanding of medical terminology
• Basic knowledge of pharmacovigilance and drug safety
• Good communication skills (English)
• MS Office proficiency

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🧠 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

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💰 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.

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📅 Interview Details

• Interview Mode: Online / HR Screening + Technical Rounds
• Selection Process:
  1. Application Screening
  2. HR Interview
  3. Technical / Safety Assessment
  4. Final Selection

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📄 Required Documents

Candidates should keep the following documents ready:

• Updated Resume (CV)
• Educational Certificates
• Nursing Degree Proof
• ID Proof (Aadhaar/PAN)
• Experience Certificates (if applicable)
• Passport-size Photograph

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📩 How to Apply

Interested candidates can apply through the official Medpace careers portal or job listing platforms.

Apply here:

https://careers.medpace.com/jobs/12662

Alternative Apply:
https://www.naukri.com/job-listings-drug-safety-specialist-clinical-safety-coordinator-medpace-clinical-research-india-navi-mumbai

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❓ FAQs

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.

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🧾 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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⚠️ Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.

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