Responsibilities:
- Determine plan of action for incoming calls
- 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
Qualifications:
- Bachelor’s degree in Healthcare related field (Nursing, Pharmacy, Pharmacology, etc.)
- Clinical experience or Clinical Research, case processing, and Post-marketing Pharmacovigilance experience is preferred
- Proficient in English
- Proficient knowledge of Microsoft® Office
- Broad knowledge of medical terminology
- Strong organizational and communication skills
