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Medical Reviewer Fixed-Term


Are you a Medical Doctor? Do you have experience in the pharmaceutical industry?

If you are, read on, we have a great opportunity for you to support one of the world’s most prestigious pharma companies. You will be part of a 100+ multicultural team, working to help create a new drug that helps humankind live freely. We are recruiting for a new project in Pharmacovigillance, which is a relatively new business area in Hungary; this will be a great chance for you to become more competitive on the job market after this one year project. We want to help you develop your career in a global environment while contributing to health safety.


  • To author Company Clinical comment (CCC) for required cases that are Suspected Unexpected Serious Adverse reaction (SUSAR).
  • To review the medical sense of the case and ensure that the company point of view is accurately reflected.
  • To serve as a point of contact for all Products related queries.
  • Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database.
  • Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database.
  • Review the company causality assessment provided by Medical Advisor.
  • Maintain knowledge of the marketed drug currently under litigation.
  • Support Medical advisor activity as and when required.


Academic Qualification:

Medical Doctor Degree

· Computer Literate ( good knowledge of MS Office)
· Sound understanding of the Drug Safety and Regulatory process.
· Good problem solving and decision making skills.
· 1 – 2 years of Experience in pharmacovigilance or clinical.
· Basic Medical Advisor training
· Drug Development/Patient Safety/Clinical experience obtained while working in industry and/or academia
· Knowledge of drug safety & clinical development.
· Knowledge of US and EU pharmacovigilance regulatory requirements
· Excellent written and verbal communication skills and ability to present and critically discuss clinical data in both internal and external discussions.
· Ability to evaluate, interpret and synthesize scientific data (analytical thinking).

*Please note this position has a 1-year fixed-term contract*

Candidate must be available to work in Hungary from Novemeber.


As our future TCSer

you will contribute to the development of a new drug so that our client can provide the best care for their customers

you will have opportunity to work with one of the Top 10 Pharma company partners.

you can use your knowledge and skills in the area of Pharmacovigilance – Drug Safety (The branch of pharmacology focused on detecting, assessing, understanding and preventing long- and short-term adverse effects of medicines.), and its regulations

  • home office.


Victoria Bernal Rivera

Email: victoria.b1@tcs.com
Cell: +36 30 198 8648


Victoria Bernal Rivera
Email: victoria.b1@tcs.com
Cell: +36 30 198 8648