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Medtronic, a global leader in healthcare technology, is hiring a Clinical Studies Support Coordinator II in Mumbai, India. This hybrid role offers a unique opportunity to contribute to clinical research, data coordination, and document management while working for a mission-driven organization that is transforming patient care worldwide.
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If you have 2+ years of experience in clinical studies or research coordination, this could be the right step to accelerate your career.
Key Responsibilities
As a Clinical Studies Support Coordinator II, you will:
- Support clinical studies by coordinating data and documents.
- Participate in the development and testing of case report forms, databases, and study reports.
- Verify study data, resolve discrepancies, and ensure timely completion of study forms.
- Process compensation and resolve related discrepancies.
- Create, organize, and maintain clinical study files and documentation.
- Assist in audits to ensure accuracy and completeness of study files.
- Communicate with internal teams and stakeholders for updates and clarifications.
- Provide guidance to new or entry-level employees as needed.
Qualifications
- Minimum Bachelor’s degree in Life Sciences, Pharmacy, or related field.
- At least 2 years of relevant experience in clinical research, data coordination, or document management.
- Strong organizational, communication, and problem-solving skills.
- Ability to work under moderate supervision with established processes.
- Familiarity with clinical data management systems and regulatory documentation preferred.
Benefits & Compensation
Medtronic offers a competitive salary package with an estimated range of ₹6,00,000 – ₹10,00,000 per year, depending on qualifications and experience. Additional benefits include:
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- Hybrid work model (office + remote flexibility).
- Comprehensive health and wellness plans.
- Professional development opportunities.
- A collaborative and purpose-driven work environment.
How to Apply
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