ARGUS-Focused Pharmacovigilance Safety Specialist

3M HEALTHCARE; Durham (NC); On-site; USD 50,100 - 125,300; Full time

Job summary

IQVIA is seeking a Safety Specialist to join the FSP team. You will process non-serious adverse event cases, enter data into ARGUS, and collaborate with the case processing team to ensure timely, regulatory-ready reports.

You bring 1–3 years in Safety or Pharmacovigilance, understand case processing workflows, and are proactive in quality and timelines. This role offers growth in a global healthcare data environment.

Qualifications

• 1–3 years of experience in Safety or Pharmacovigilance.
• Solid understanding of case processing workflows and safety database operations.
• Familiarity with ARGUS or similar safety systems.
• Commitment to quality, timelines, and continuous improvement.

Responsibilities

• Process non-serious adverse event cases with accuracy and efficiency.
• Enter and transfer data from AE forms into ARGUS following local affiliate model.
• Collaborate with the case processing team who finalize cases in ARGUS and generate reports.
• Support timely submission of safety reports to the FDA and global authorities.

Skills

Case processing

Pharmacovigilance

Data entry

Team collaboration

Tools

ARGUS

Job description

IQVIA is seeking a Safety Specialist to join the FSP team. You will process non-serious adverse event cases, enter data into ARGUS, and collaborate with the case processing team to ensure timely, regulatory-ready reports.

You bring 1–3 years in Safety or Pharmacovigilance, understand case processing workflows, and are proactive in quality and timelines. This role offers growth in a global healthcare data environment.