Search Results: 4 vacancies
Purpose of the role: This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with...
...operations and reporting, adhering to Good Clinical Practice (GCP) guidelines.
Qualifications and Experience:
MBBS, MD, or Pharmacology degree from a recognized institution
1. 15+ years of experience in clinical research and regulatory affairs within the...
...A. Qualification:
- MBBS degree approved by MCI (Medical Council of India.)
- Master's Degree. M.D Pharmacology / MD in Medicine
- Understanding of clinical research process and ICH GCP & BA/BE studies
- Basic understanding of the drug development process
B. Experience...
...Prepare and review clinical documents that are part of regulatory submission including but not limited
to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval
Documents across the Therapeutic Areas.
1. Quality check of the...
