- Manage end-to-end Clinical Data Management activities for clinical studies.
- Handle study setup, data review, query management, data cleaning and database lock.
- Work on EDC/CDMS systems such as Medidata Rave, Oracle InForm or similar tools.
- Perform data reconciliation with safety, laboratory and other external data.
- Coordinate with Clinical Operations, Statistics, SAS and other cross-functional teams.
- Communicate with clients/sponsors and provide study updates.
- Support study timelines, quality and compliance with GCP and SOPs.
- Lead/guide Clinical Data Management team members and support issue resolution.
- Participate in UAT,
edit check review and database validation activities.
Qualification: Bachelors/Masters degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology or related field. Preferred: Experience in CRO/Pharma and end-to-end clinical study management.