Actalent is hiring a Drug Safety Associate for a hybrid role in Clayton, NC. You will independently contribute to pharmacovigilance, processing adverse event data, ensuring GCP compliance, and collaborating with clinical, scientific, and operations teams.
The role requires 2–3 years in a clinical setting or related training, familiarity with safety databases (ARGUS), and strong organizational skills to manage multiple cases and deliver timely safety deliverables.
#J-18808-LjbffrDrug Safety Specialist - Hybrid, Data-Driven AE Tracking in iowa at Unknown Company
This position is listed as full time and hybrid.