Pharmacovigilance Associate II

Job Summary

A company is looking for an Associate II, Pharmacovigilance.

Key Responsibilities

• Author Safety Management Plans for assigned studies
• Review incoming SAE data for completeness and accuracy, and perform data entry in the Safety Database
• Generate regulatory reports and prepare periodic safety reports as needed

Required Qualifications

• Bachelor's degree in a science-related field, nursing, or equivalent
• Minimum of 1 year of pharmacovigilance experience (pre-approval clinical trials)
• Good understanding of medical and scientific terminology and international regulations
• Computer literacy and strong working knowledge of MS Office applications
• Excellent organization skills and ability to handle multiple competing priorities