Drug Safety Specialist/ Clinical Safety Coordinator
Core
Handling and processing adverse events from clinical trials and post-marketing surveillance sources.
Role type
Clinical Safety Coordinator (Pharmacovigilance)
Builds
Safety narratives and safety data reports for clinical research clients
Domain
Clinical Research / Pharmacovigilance
Required skills
Adverse event case processing, Safety narrative writing, Medical terminology knowledge, Microsoft Office proficiency, Regulatory compliance knowledge
Preferred skills
Clinical research experience, Post-marketing pharmacovigilance experience, Investigative site collaboration
Technologies
Microsoft Office
Responsibilities
Collect, process, and track incoming adverse and serious adverse events; Write safety narratives; Report on various safety data; Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Seniority
Entry to Mid-level, hands-on IC
