Drug Safety Specialist/ Clinical Safety Coordinator
Medpace, a full-service clinical contract research organization, is seeking a Clinical Safety Coordinator based in India. The role focuses on handling and processing adverse events from clinical trials and post-marketing surveillance, including writing safety narratives and ensuring regulatory compliance. Candidates must have a healthcare-related degree and knowledge of medical terminology. This is an office-based role within their Clinical Safety department.
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Experience
Experience not specified
Function
Healthcare Services
Work mode
Onsite, India
Company
Tier 2
What you will work on
Medpace, a full-service clinical contract research organization, is seeking a Clinical Safety Coordinator based in India. The role focuses on handling and processing adverse events from clinical trials and post-marketing surveillance, including writing safety narratives and ensuring regulatory compliance. Candidates must have a healthcare-related degree and knowledge of medical terminology. This is an office-based role within their Clinical Safety department.
TAL's take
Solid tier-2 global CRO offering well-defined specialized clinical research role with clear responsibilities.
Clear, well-defined clinical role with specific responsibilities in pharmacovigilance and adverse event processing.
Must haves
- Bachelor's degree in Healthcare related field
- Proficient English
- Proficient knowledge of Microsoft Office
- Broad knowledge of medical terminology
- Strong organizational and communication skills
Tools and skills
About the company
Established global CRO with thousands of employees and strong industry reputation.