Clinical Safety Coordinator
On-site
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 development
Domain
Clinical research / Pharmacovigilance
Required skills
Adverse event processing, Safety narrative writing, Medical terminology, Microsoft Office, Organizational skills
Preferred skills
Nursing background, Clinical research experience, Post-marketing Pharmacovigilance experience
Technologies
Microsoft Office
Responsibilities
Determine plan of action for incoming calls, Collect and track incoming events, Write safety narratives, Report on safety data, Collaborate with internal departments and clinical research sites
Seniority
Mid-level, hands-on IC
