Medtronic is hiring for the position of Clinical Studies Spt Coord II in Mumbai, Maharashtra, India. This is a full-time, remote job opportunity involving clinical study data coordination, clinical documentation, study database support, and discrepancy resolution.
The position is listed under job requisition ID R77059 and requires a minimum of two years of relevant experience.
Job Details
| Particulars | Details |
|---|---|
| Company | Medtronic |
| Job Title | Clinical Studies Spt Coord II |
| Job Requisition ID | R77059 |
| Job Location | Mumbai, Maharashtra, India |
| Work Mode | Remote |
| Job Type | Full-time |
| Experience | Minimum 2 years of relevant experience |
| Job Category | Clinical Studies Support |
| Posting Date | October 14, 2026 |
Positions
Medtronic is recruiting for the Clinical Studies Support Coordinator II position. The role supports clinical studies through data coordination, study documentation, database activities, and clinical study file management.
Responsibilities
Selected candidates may be responsible for the following activities:
- Clinical Data Coordination: Participate in developing and testing case report forms, study reports, and study databases according to protocol requirements.
- Data Quality Management: Ensure timely and accurate completion of data forms and verify clinical study data.
- Discrepancy Resolution: Generate, manage, and resolve data discrepancies.
- Compensation Processing: Process compensation and identify and resolve compensation discrepancies.
- Clinical Documentation: Create, maintain, organize, and distribute clinical study documents.
- Study File Management: Maintain clinical study files and support document coordination.
- Audit Support: Assist with periodic audits of clinical study files to ensure completeness and accuracy.
- Process Improvement: Identify routine work-process issues and suggest solutions within the assigned area.
Eligibility and Qualifications
Candidates should meet the following experience requirement:
- Minimum of 2 years of relevant experience.
- Knowledge of systems and procedures gained through prior work experience or education.
- Ability to perform administrative and operational assignments under moderate supervision.
The role requires established working knowledge of relevant procedures and the ability to manage routine clinical study support activities.
Required Skills
The responsibilities outlined in the job description indicate the importance of the following capabilities:
- Clinical study data coordination
- Case report form and study database support
- Clinical data verification and discrepancy management
- Clinical documentation and study file maintenance
- Document organization and distribution
- Audit preparation and file completeness checks
- Administrative coordination and problem-solving
- Internal communication and collaboration
Job Location and Work Mode
The position is listed as remote, with Mumbai, Maharashtra, India, as the associated location. It is a full-time opportunity within Medtronic’s clinical studies support function.
