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Regulatory Operations Associate
Precision Medicine Group
Bengaluru / Bangalore
Not Disclosed
0 - 5 Years
Full Time - Permanent
Views:249
Applicants:3
Posted on 16 Jun, 2025
In Office
Job Description | Responsibilities
- Upload, organize, and maintain regulatory documents within applicable regulatory authority submissions portals (e.g. Clinical Trial Information System (CTIS), FDA eGateway, Common European Submissions Platform (CESP), etc.).
- Coordinate the redaction of confidential and proprietary information in regulatory documents
- Support the creation .
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Other
- Job Role - Other
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
(MS Office/ Office 365)
Regulatory Operations Associate
pharmaceutical
or biotech company.
