Join Medpace as a Clinical Safety Coordinator in Navi Mumbai! Process adverse events, ensure compliance, and grow your pharmacovigilance career. Apply now for this nursing/pharmacy role.
Introduction
Medpace, a leading global CRO, is hiring a Clinical Safety Coordinator in Navi Mumbai to manage adverse event reporting for clinical trials and post-marketing surveillance. This office-based role offers career growth in pharmacovigilance for healthcare graduates with clinical research experience.
Key Responsibilities
- Process and track adverse events (AEs/SAEs) from trials and post-marketing data.
- Draft safety narratives and generate regulatory reports.
- Collaborate with cross-functional teams for GCP compliance.
- Handle safety data using Microsoft Office and pharmacovigilance databases.
Qualifications
- Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or related healthcare field.
- 1+ years’ experience in clinical research/pharmacovigilance (preferred).
- Medical terminology proficiency and strong English communication skills.
- Familiarity with ICH-GCP guidelines and case processing workflows.
Benefits at Medpace
- Flexible work policies and competitive salary (₹4–8 LPA, based on experience).
- Structured career growth in a Forbes-recognized midsize company.
- Health wellness programs and employee appreciation events.
