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.

As part of your work with beginning-to-end trial experience, you will ​​​expand your knowledge and experience working on clinical trials through every stage of drug development. This includes management and oversight of all contracted services. 

What area interests you?

  • Safety Administrator and Specialist
  • Safety Reporting Administrator and Specialist
  • Safety Administrator Manager
  • Manager, Director and Assistant Director
  • Medical Director

Hear from our colleagues:

"Without exaggerating, this has been one of the best decisions in my life. I love the fact that as a people manager I’m able to mentor and help my direct reports grow continuously. With Pharmacovigilance, no single day is the same. There is always something positive and exciting happening in our global department. I am truly happy and humbled to be part of our organization. If you are a professional interested in a career within pharmaceutical product development, healthcare or patient safety – this is the place to be!"
Lubomir, Manager, Pharmacovigilance, Sofia, Bulgaria
"Thermo Fisher has a great team spirit, which is hard to find. The company appreciates people, invests in them and provides opportunities for growth and development. Every day there is something new to learn!" 
Asimina, Manager, Pharmacovigilance, Athens, Greece
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