Location: Nationwide
Compensation: To Be Discussed
Staff Reviewed: Tue, Sep 12, 2023
This job expires in: 20 days
Job Summary
A company is looking for a PV Operations Consultant in the Life Sciences & Technology industry.
Key Responsibilities:
- Collect, review, and process adverse event (AE) information in compliance with regulations and guidelines
- Conduct and/or review/approve periodic reconciliation of serious adverse events (SAEs) between drug safety and clinical trial databases
- Prepare agenda, minutes, and reports for monthly signal meetings
Qualifications:
- Experience in Pharmacovigilance (PV) Operations and global regulations
- Knowledge of Serious Adverse Events (SAEs) and SUSARs
- Experience in oncology is preferred
- Bachelor's degree in a related field
- Experience working in small to mid-sized companies is preferred