Safety Specialist - 1

IQVIADurham, NC
16d

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. You’ll be at the heart of our safety operations, ensuring that every case is handled with precision, speed, and care.

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
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