Position: Associate PV / Sr. Associate PV
Experience: 0-4 years

Key Responsibilities:

• Manage Adverse Events related to company products, including generating, processing, and tracking follow-up requests.
• Conduct global literature surveillance.
• Develop PSUR, RMP, and other safety reports.
• Support the management of the Medical Information System.
• Maintain the Safety Database.
• Develop, review, and update SOPs and Working Instructions.
• Stay up-to-date with company procedures & international pharmacovigilance regulations.

Qualifications:

• B.Pharm./M.Pharm. (Pharmacy graduates)

About Us:
Kathin – A Healthy Future at Evolet

We are committed to ensuring a safe and healthy future for all. If you are passionate about pharmacovigilance and eager to grow in a dynamic environment, we encourage you to apply.

How to Apply:
Send your resume to vacancy@evolet.in

Apply Now!
Join us in our mission to make a difference.