Work Schedule: Standard Office Hours (40 per week).

As part of the Thermo Fisher Scientific team you will discover meaningful work that makes a positive impact on a integral scale. Our detailed, goal‑oriented pharmacovigilance colleagues manage the safety profile of new drugs in clinical trials, oversee case‑processing activities through all phases of development, and perform regulatory reporting and medical monitoring.

• Provide medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed.
• Attend and present at investigator and sponsor meetings, provide medical consultation to clients, investigators and project team members, and support business development activities.
• Provide medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g., PBRER, PSUR, DSUR) as well as other cl...