Safety Specialist

IQVIADurham, NC

About The Position

Step into a role where your attention to detail, passion for patient safety, and drive for excellence truly make an impact. The FSP team at IQVIA is looking for a dynamic Safety Specialist ready to grow, collaborate, and help deliver high‑quality pharmacovigilance support for global clients. If you thrive in a fast‑paced environment and love the idea of contributing to safer healthcare outcomes, this is your moment.

Requirements

  • 1–3 years of experience in Safety or Pharmacovigilance.
  • A solid understanding of case processing workflows and safety database operations.
  • Familiarity with ARGUS or similar safety systems.
  • A commitment to quality, timelines, and continuous improvement.
  • A proactive, positive mindset and the ability to thrive in a collaborative team environment.

Responsibilities

  • Processing non‑serious adverse event cases with accuracy and efficiency.
  • Entering and transferring data from AE forms in solicited programs into ARGUS , following a local affiliate model rather than a centralized ARGUS setup.
  • Collaborating closely with the case processing team , who will finalize cases in ARGUS, perform medical coding, and generate regulatory‑ready reports.
  • Supporting the timely submission of safety reports to the FDA and other global regulatory authorities .

Benefits

  • health and welfare and/or other benefits
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