Pharma Jobs

Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required 

Pharmacovigilance (PV) Associate will be responsible for all assigned Clinical Safety and post-marketing PV activities. The PV Associate will be part of the newly developed, lean and efficient, Global Safety Data Management team

More than 2 years experience in pharmaceutical industry or clinical research organization or health care experience, as a Medical Data Reviewer, Medical Monitor or similar roles. Basic knowledge in planning, executing, and reporting global clinical studies.

M.Pharm or M.S. in Pharmacology with 2–5 years of research experience in academic or industrial R&D settings

Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment. Ability to handle multiple tasks in a timely and professional manner under demanding conditions.

B.Pharmacy OR 10+2 with Science and Diploma in Pharmacy. Preference will be given to the Ex-Servicemen.

Director/Principal: Ph.d in relevant discipline, Assistant professor for B.Pharm: M.Pharm in respective Specialization with min 2+ year of experience, Lecturer for D.Pharm: B.Pharm in respective specialization with min 3+ year of experience

Post Graduation in Basic/Applied Sciences/ Engineering/ Pharmacy/ Technology (with 60% aggregate marks for GEN and 55% aggregate marks for SC/ST candidates) from a UGC recognized University / Institute / Autonomous bodies