• Support clinical studies through coordination of study data and documentation
• Assist in development, testing, and maintenance of case report forms (CRFs), databases, and study reports
• Verify clinical study data, resolve discrepancies, and ensure timely completion of study forms
• Process subject compensation and resolve related discrepancies
• Create, organize, and maintain clinical study files in compliance with regulatory requirements
• Support internal and external audits to ensure accuracy and completeness of study documentation
• Communicate with internal teams and stakeholders to provide updates and clarifications
• Provide guidance and support to new or entry-level team members as required
• Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline
• Minimum 2 years of experience in clinical research, clinical studies coordination, data coordination, or document management
• Experience working with clinical study documentation and data verification processes
• Strong organizational, communication, and problem-solving skills
• Ability to work under moderate supervision using established processes
• Familiarity with clinical data management systems and regulatory documentation
• Attention to detail and ability to manage multiple tasks effectively
Medtronic is a global leader in healthcare technology, committed to alleviating pain, restoring health, and extending life. With a strong focus on innovation and patient-centered solutions, Medtronic supports clinical research that drives safe, effective, and transformative medical technologies worldwide.
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