Clinical Studies Support Coordinator II at Medtronic manages data coordination, document organization, and administrative support for clinical studies. The role involves developing case report forms, verifying study data, maintaining clinical study files, and resolving discrepancies under moderate supervision.

Responsibilities

- Develop and test case report forms, study reports, and databases per protocol requirements
- Verify study data accuracy and manage data discrepancies to resolution
- Create and organize clinical study files and oversee document distribution
- Process compensation records and identify compensation-related discrepancies
- Conduct periodic audits of clinical study files for completeness and accuracy

Requirements

- Minimum 2 years of relevant clinical operations or administrative experience
- Full knowledge of clinical study systems, procedures, and databases
- Proficiency in case report form development and data management
- Robust organizational and documentation skills
- Ability to work with moderate supervision and make process adjustments

📌 Clinical Studies Spt Coord II (Mumbai)
🏢 Medtronic
📍 Mumbai