Drug Safety Associate (Life Sciences Degrees)
Core
Collect, process, and track serious adverse event (SAE) reports; generate safety narratives and queries; perform quality control of safety cases.
Role type
Clinical Safety Coordinator
Builds
Safety cases and narratives for clinical trials and post-marketing surveillance
Domain
Life Sciences / Clinical Research
Required skills
SAE report processing, safety narrative generation, safety database data entry, quality control of safety cases, medical terminology knowledge, Microsoft Office proficiency
Preferred skills
None stated
Technologies
Microsoft Office
Responsibilities
Collect, process, and track serious adverse event (SAE) reports; Generate safety narratives and queries; Perform quality control of safety cases; Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Seniority
Entry-level, individual contributor
