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💼 Clinical Safety Coordinator
🏢 Company: Medpace📍 Location: Navi Mumbai, India
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
🧪 Experience: 1+ Years
📝 Job Type: Full-Time | Pharmacovigilance | On-site
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Medpace
Medpace is a leading global Clinical Research Organization (CRO) recognized for excellence in clinical trial management and regulatory compliance. With a presence in over 40 countries, Medpace partners with sponsors to accelerate drug, biologic, and device development, ensuring high-quality clinical research outcomes.
📌 Key Responsibilities
- ✔ Process and track adverse events (AEs/SAEs) from clinical trials and post-marketing surveillance.
- ✔ Draft safety narratives and prepare regulatory safety reports.
- ✔ Collaborate with cross-functional teams to maintain GCP compliance.
- ✔ Manage safety data using Microsoft Office and pharmacovigilance databases.
✅ Eligibility & Skills
- ✅ Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or related healthcare field.
- ✅ 1+ years’ experience in clinical research or pharmacovigilance (preferred).
- ✅ Proficiency in medical terminology and strong English communication skills.
- ✅ Familiarity with ICH-GCP guidelines and case processing workflows.
🎁 Why Join Medpace?
- 🌐 Work with a Forbes-recognized midsize global CRO.
- 📈 Structured career growth opportunities.
- 💼 Flexible work policies and competitive salary (₹4–8 LPA).
- 🤝 Employee wellness programs and appreciation events.
📌 Note Before You Apply:
Highlight your experience in pharmacovigilance, adverse event processing, and regulatory reporting. Showcase your knowledge of ICH-GCP and medical terminology to stand out in your application.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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