Remote Clinical Safety Specialist — Adverse Event & Compliance

A leading medical device company seeks a Clinical Safety Specialist (Remote) in Irvine, California. The candidate will ensure accurate safety assessments of adverse events across clinical studies and registries. Responsibilities include collaborating with internal teams, reviewing adverse events using MedDRA, and ensuring compliance with global safety reporting. Ideal candidates should have a Bachelor’s degree and at least 2 years of clinical research experience.

Excellent analytical skills and knowledge of GCP are preferred. Competitive salary range and benefits offered.
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