Are you passionate about advancing healthcare through clinical research? Medtronic, a global leader in healthcare technology, is hiring Clinical Studies Support Coordinators (Level II and III) in Mumbai, Maharashtra. These hybrid roles offer a unique opportunity to contribute to life-changing medical innovations while working with a dynamic, mission-driven team dedicated to alleviating pain, restoring health, and extending lives. If you’re ready to make a difference in the healthcare industry, explore these exciting career opportunities at Medtronic.
Job Responsibilities
As a Clinical Studies Support Coordinator at Medtronic, you’ll play a vital role in ensuring the success of clinical studies. Your responsibilities will include:
- Data Coordination: Develop and test case report forms, study reports, and databases based on protocol requirements. Ensure timely and accurate completion of data forms, verify study data, and resolve data discrepancies.
- Document Coordination: Create and manage clinical study files, oversee document organization and distribution, and assist with periodic audits to ensure completeness and accuracy.
- Compensation Processing: Process compensation for study participants and resolve any discrepancies (where applicable).
- Support and Collaboration: Provide administrative and clerical support to clinical study teams, ensuring smooth execution of tasks under moderate (Level II) or limited (Level III) supervision.
- Innovation and Problem-Solving: Identify and propose solutions to improve processes and address routine challenges in clinical study operations.
Level III coordinators will also provide guidance and training to entry-level employees, contributing to team development and operational excellence.
Qualifications and Requirements
To excel in these roles, candidates must meet the following criteria:
- Experience:
- Level II: Minimum of 2 years of relevant experience in clinical research or administrative support.
- Level III: Minimum of 4 years of relevant experience, with a strong background in operational systems and clinical study processes.
- Education: Practical knowledge of systems and procedures gained through prior work experience or education.
- Skills:
- Proficiency in data management and document coordination.
- Strong organizational skills and attention to detail.
- Ability to work under supervision, with Level III requiring the ability to perform non-routine tasks and provide training.
- Effective communication skills for internal and external collaboration.
- Physical Requirements: Ability to perform standard office tasks, including prolonged computer use and document handling.
Benefits of Working at Medtronic
Medtronic values its employees and offers a competitive and flexible benefits package, including:
- Competitive Salary: A rewarding compensation plan reflecting your contributions.
- Comprehensive Benefits: Health, wellness, and financial benefits to support you at every career and life stage.
- Career Growth: Opportunities for professional development and lifelong learning in a global healthcare technology leader.
- Inclusive Culture: A dynamic, diverse workplace that fosters innovation and collaboration.
- Impactful Work: Contribute to Medtronic’s mission to alleviate pain, restore health, and extend life for patients worldwide.
How to Apply
Application Link for Clinical Studies Support Coordinator II
Application Link for Clinical Studies Support Coordinator III
