Pharmacovigilance Associate II

A company is looking for an Associate II, Pharmacovigilance.

Key Responsibilities

Author Safety Management Plan for assigned studies

Review incoming SAE data for completeness and accuracy

Generate regulatory reports and perform safety submissions as needed

Required Qualifications, Training, and Education

Bachelor's degree in a science-related field, nursing, or equivalent

Minimum of 1 year of pharmacovigilance experience (pre-approval clinical trials)

Computer literacy and strong working knowledge of MS Office applications

Ability to work independently and prioritize effectively

Strong understanding of medical and scientific terminology and international regulations