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Safety Specialist II

Company: VirtualVocations
Location: Fullerton
Posted on: November 19, 2024

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, Irvine , Safety Specialist II, Other , Fullerton, California

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