Pharmacovigilance Associate at ICON – Remote/Hybrid Role, Apply Now!
Are you looking to launch or advance your career in pharmacovigilance? ICON plc is hiring a Pharmacovigilance Associate to join its dynamic Post-Marketing and Medical Device Safety Team. Based remotely or in a hybrid setup from Blue Bell, PA or Raleigh, NC, this role is ideal for candidates with 6–12 months of experience in drug safety, especially in case processing and safety database handling (ARGUS preferred). Contribute to patient safety by analyzing adverse events and supporting global regulatory submissions, all while working with one of the top CROs in the world.
- Collecting and reviewing adverse event reports for accurate and timely reporting
- Conducting signal detection and risk assessment activities
- Collaborating with cross-functional teams as Pharmacovigilance Associate
- Maintaining knowledge of pharmacovigilance regulations
- Assisting in the preparation of safety reports and regulatory submissions
Your profile:
- 6-12 months experience in pharmacovigilance or drug safety
- Experience in case processing and writing narratives in ARGUS or similar safety database
- Strong analytical skills and attention to detail as Pharmacovigilance Associate
- Excellent communication and interpersonal skills
- Bachelor’s degree in life sciences, pharmacy, or related field
Keywords: Pharmacovigilance Associate, ICON, Drug Safety, Remote, Hybrid, Job, Blue Bell, Raleigh, Clinical Research, Healthcare, Pharmaceutical, ARGUS, Signal Detection, Risk Assessment
