You will perform day-to-day Pharmacovigilance activities including data entry, coding, and assessment of adverse events within a highly regulated environment
Job Summary
You will perform day-to-day Pharmacovigilance activities including data entry, coding, and assessment of adverse events within a highly regulated environment.
The role requires maintaining medical understanding of therapeutic areas while reviewing cases for quality, consistency, and accuracy.
Join a global team at Thermo Fisher Scientific that values passion, innovation, and a commitment to scientific excellence.
Matching Summary
You will perform day-to-day Pharmacovigilance activities including data entry, coding, and assessment of adverse events within a highly regulated environment.