clinical data coordinator II

Roles and Responsibilities :

• Coordinate clinical trial data management activities, ensuring timely and accurate delivery of high-quality data.
• Conduct site visits to monitor patient enrollment, data collection, and study procedures compliance.
• Collaborate with cross-functional teams to resolve issues related to study setup, protocol deviations, and closeout.
• Ensure all documentation is complete, accurate, and compliant with regulatory requirements.

Job Requirements :

• 2-5 years of experience in Clinical Data Management (CDM) or a related field.
• Strong understanding of Medidata Rave or similar eCRF systems for managing clinical trials.
• Experience working on startup projects or early-stage pharmaceutical companies preferred.
• Excellent conducting skills with ability to work independently at client sites.