Clinical Research Source Writer - Precise, Compliant Docs

A clinical research organization in Toms River is seeking a detail-oriented professional responsible for creating source documentation for clinical trials. The role involves editing, tracking, and revising documents in compliance with ICH and GCP guidelines. Candidates should have a Bachelor's degree and experience in clinical research, as well as strong writing and organizational skills. This position offers competitive compensation and benefits after 30 days of employment. #J-18808-Ljbffr