Karnataka

Works closely with the Global Regulatory Lead, Regulatory Affairs Manager providing the submission strategy and with the Submission Manager executing the submissions.

In this role, you will perform coding activities on the assigned project in a timely and efficient manner, code the Medical Conditions and Medication terms in the Coding tool, generate Queries to clarify in order to facilitate coding, and participate in study related meetings as needed.

First class bachelor degree in Pharmacy, relevant subject Pharmacology from a recognized university in relevant field.

Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions.

The purpose of the Quality Medical Reviewer role in Medical Affairs is to review and approve medical and promotional materials to ensure they are medically accurate and interpreted correctly based on the review of references, citations and data available.

Post graduate Degree or PhD in Life Sciences, Pharmacology and Biomedical engineering with experience three years in conducting large scale intervention studies.

Market research and analysis of CDMO landscape, Biologics, Biosimilars and Small Molecules business. Refer databases, news, articles etc and generate leads for potential business, newer technologies etc. Reach out to leads and present about One Source Capabilities.

To provide undergraduate engineering or postgraduate science student with an opportunity to engage in advance research and gain hands-on experience in the project

Responsible for analysis and documentation of Bioassay samples of finished products and stability samples.