Safety Specialist II
Company: VirtualVocations
Location: Fullerton
Posted on: November 19, 2024
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Job Description:
A company is looking for a Safety Specialist II to manage the
intake and reporting of Serious Adverse Event (SAE) reports in
clinical research.
Key Responsibilities
Process and evaluate incoming SAE reports according to regulatory
guidelines and company SOPs
Interface with sponsors and team members to design and implement
safety collection tools and reporting systems
Mentor or train new Pharmacovigilance staff and participate in the
development of safety reporting plans
Required Qualifications
4-year college degree in Pharmacy, Nursing, scientific, or
healthcare discipline
3-5 years of clinical trial and Pharmacovigilance/Drug Safety
experience
Health care professional (i.e., RN, BSN, MD, PharmD)
Hands-on experience with global safety databases and SAE case
processing
Proficient in MedDRA and WHO Drug coding
Keywords: VirtualVocations, Tustin , Safety Specialist II, Other , Fullerton, California
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