Global Pharmacovigilance Specialist - Lead SAE Data & Reports

Worldwide Clinical Trials; Durham (NC); On-site; USD 50,000 - 99,000; Full time

Job summary

Worldwide Clinical Trials is seeking an Associate in Pharmacovigilance in the United States. You will manage SAE data collection, review for completeness, and perform data entry in safety databases, with support from senior PV staff on small to moderate studies.

The role requires a Bachelor’s degree in a science field or nursing, 1 year of PV experience, and strong MS Office skills. You will work in a global environment, travel if needed, and contribute to regulatory safety submissions.

Qualifications

• Bachelor’s degree in a science‑related field, nursing, or equivalent.
• Minimum of 1 year of pharmacovigilance experience (pre‑approval clinical trials).
• Equivalent combination of relevant education and experience.

Responsibilities

• Author Safety Management Plan for assigned studies.
• Review incoming SAE data for completeness and accuracy.
• Perform data entry in the Safety Database and track safety information.

Skills

Medical terminology

Regulatory awareness

Excellent communication

Independent worker

Multi-tasking

Education

Bachelor’s degree in science or nursing

Tools

Excel

PowerPoint

Word

Job description

Worldwide Clinical Trials is seeking an Associate in Pharmacovigilance in the United States. You will manage SAE data collection, review for completeness, and perform data entry in safety databases, with support from senior PV staff on small to moderate studies.

The role requires a Bachelor’s degree in a science field or nursing, 1 year of PV experience, and strong MS Office skills. You will work in a global environment, travel if needed, and contribute to regulatory safety submissions.