Manager, Regulatory Clinical Trials
Location
Gurgaon, India
Job Type
Full-time
Category
other-general
Posted
June 06, 2026
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice (https://jobs.takeda.com/privacynotice) and Terms of Use (https://www.takeda.com/terms-and-conditions/) . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**OBJECTIVES/PURPOSE** : Manager, Clinical Regulatory Affairs (India) is responsible for managing regulatory activities for clinical trials in India and managing/ supporting preparation, submission, Q&A and maintenance of Clinical Trial Applications (CTAs), amendments, and responses to Health Authority (HA) queries at LOC level, and supports HA interactions including Subject Expert Committee (SEC) preparation. This position works in close alignment with the Global/International Regulatory Clinical Trials team, GDO,...
**Job Description**
**OBJECTIVES/PURPOSE** : Manager, Clinical Regulatory Affairs (India) is responsible for managing regulatory activities for clinical trials in India and managing/ supporting preparation, submission, Q&A and maintenance of Clinical Trial Applications (CTAs), amendments, and responses to Health Authority (HA) queries at LOC level, and supports HA interactions including Subject Expert Committee (SEC) preparation. This position works in close alignment with the Global/International Regulatory Clinical Trials team, GDO,...