Opportunity to work in Pharmacovigilance


About Company: 

Bioclinica is specifically structured to create clarity in the clinical trial process—so you can make better decisions. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. The company serves more than 400 pharmaceutical, biotechnology, and device organizations – including all of the top 20 – through a network of offices in the U.S., Europe and Asia.

Department: Pharmacovigilance

Post:  Sr. Drug Safety Associate

Qualification: B.Pharmacy, M.Pharmacy 

Experience: 4-5 years

 Job Description: 

  • Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD).
  • Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
  • Review and evaluate AE case information to determine required action based on and following internal policies and procedures.
  • Process all incoming cases in order to meet timelines.

 Salary: Not disclosed 

 Location: Mysore, Karnataka

Interested candidates can apply directly on company website  https://www.bioclinica.com/about/careers

Posted by Placement Manager IGMPI

Email: corporate.resources@igmpi.org
Telephone: +91 9599912742.