Clinical Studies Support Coordinator II

Roles & Responsibilities
• Support clinical studies by coordinating study data and essential documents
• Participate in the development and testing of case report forms (CRFs), databases, and study reports
• Verify study data, resolve discrepancies, and ensure timely completion of study documentation
• Process subject compensation and resolve related discrepancies
• Create, organize, and maintain clinical study files and regulatory documentation
• Assist during internal and external audits to ensure accuracy and completeness of study records
• Communicate with internal teams and stakeholders for study updates and clarifications
• Provide guidance and support to new or entry-level team members
• Ensure compliance with established clinical research processes and regulatory requirements

Qualification
• Bachelor's degree in Pharmacy
• Bachelor’s degree in Life Sciences or a related field

Experience
• Minimum 2 years of relevant experience in clinical research, data coordination, or document management

Skills
• Strong organizational and time management skills
• Good written and verbal communication abilities
• Problem-solving and analytical skills
• Ability to work under moderate supervision with structured processes
• Familiarity with clinical data management systems and regulatory documentation preferred

About the Company
Medtronic is a global leader in healthcare technology, focused on developing innovative medical solutions that improve patient outcomes worldwide. The company operates across multiple therapeutic areas and is committed to advancing healthcare through research, collaboration, and technology-driven solutions.