Clinical Studies Support Coordinator III
Location: Mumbai, Maharashtra, India (Remote)
Job Type: Full-Time
Job ID: R55397
About the Role
Medtronic is seeking a Clinical Studies Support Coordinator III to provide advanced operational and data support for global clinical studies. This role focuses on clinical data management, document coordination, and administrative support, with increased autonomy and responsibility compared to entry-level positions. The Coordinator III will also mentor and train junior team members, contributing to process improvements and high-quality study execution.
This role is suitable for professionals with 4+ years of experience in clinical operations, data management, or study coordination who are looking to take the next step in a leading global medical technology company.
Key Responsibilities
Clinical Data Management:
Participate in development and testing of case report forms (CRFs), study reports, and study databases in line with protocol requirements.
Verify and ensure timely completion of study data, manage and resolve discrepancies.
Support compensation processes, including reconciliation of discrepancies.
Document Coordination:
Create, organize, and maintain clinical study files.
Oversee distribution of study documents and assist with audits for completeness and compliance.
Operational Support & Process Improvement:
Perform a variety of non-routine administrative and clerical tasks.
Propose solutions to improve workflow effectiveness and address operational challenges.
Support special projects or assignments as needed.
Leadership & Mentorship:
Provide guidance, coaching, and training to junior team members.
Share knowledge and best practices to enhance team performance.
Communication & Collaboration:
Liaise with internal and external stakeholders to provide and obtain information of moderate importance.
Communicate effectively across cross-functional teams to support study execution.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, or related field.
Minimum 4 years of experience in clinical operations, clinical study coordination, or data management.
Strong organizational skills with attention to detail and problem-solving capabilities.
Ability to work independently while providing leadership and mentorship to junior staff.
Proficiency in Microsoft Office and clinical data systems.
Excellent written and verbal communication skills in English.
What Medtronic Offers
Competitive salary and flexible benefits package.
Eligibility for the Medtronic Incentive Plan (MIP).
Opportunity to work remotely while supporting global clinical operations.
Exposure to advanced clinical trial processes and regulatory compliance standards.
Career growth opportunities within a leading healthcare technology organization.
About Medtronic
Medtronic is a global leader in medical technology, dedicated to alleviating pain, restoring health, and extending life. With over 95,000 employees worldwide, Medtronic combines innovation, expertise, and compassion to solve the world’s most challenging healthcare problems.
At Medtronic, you can advance your career while making a tangible impact on patients’ lives, collaborating with diverse teams and contributing to the execution of critical clinical studies.
Apply today to join a high-performing team driving innovation in clinical research and healthcare solutions.
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