Job Title: Clinical Studies Support Coordinator III
Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Job ID: R47514
Posted: 30+ Days Ago
Company Overview:
Medtronic is a global healthcare technology leader dedicated to alleviating pain, restoring health, and extending life. With over 95,000 employees worldwide, we drive innovation to solve complex healthcare challenges and deliver solutions that make a real difference in patients’ lives.
Position Overview:
We are seeking an experienced Clinical Studies Support Coordinator III to provide essential operational and administrative support for clinical studies. The ideal candidate will have a minimum of 4 years of relevant experience and will play a key role in ensuring accurate data management, document coordination, and smooth execution of clinical trials.
Key Responsibilities:
Data Coordination: Participate in the development and testing of case report forms (CRFs), study reports, and study databases according to protocol requirements. Ensure timely completion of data forms, verify study data, and manage data discrepancies.
Compensation Processing: Process study-related compensation and resolve any discrepancies.
Document Management: Create, organize, and maintain clinical study files. Oversee distribution of study documents and assist with periodic audits for accuracy and completeness.
Support special projects or assignments as required, providing high-quality administrative support to clinical study teams.
Mentor and provide guidance to junior team members on operational procedures and best practices.
Career Level & Impact:
Seasoned individual contributor with limited supervision.
Supports day-to-day objectives that significantly impact study operations.
Expected to propose solutions independently for manager review and contribute to process improvements.
Required Qualifications & Experience:
Bachelor’s degree in Life Sciences, Pharmacy, or a related field (or equivalent international qualification).
Minimum 4 years of experience in clinical study support, clinical operations, or related administrative roles.
Broad practical knowledge of operational systems, data management, and clinical study documentation.
Strong organizational, analytical, and problem-solving skills.
Effective communication skills to collaborate with internal and external stakeholders.
Benefits & Compensation:
Competitive salary with a flexible benefits package.
Eligible for the Medtronic Incentive Plan (MIP).
Opportunities for professional development and career growth.
Supportive work environment emphasizing employee well-being and engagement.
Why Medtronic:
Join a company committed to healthcare innovation and excellence. Medtronic empowers employees to make meaningful contributions to patient outcomes while fostering professional growth in a dynamic and inclusive environment.
Apply Today:
If you are an experienced clinical operations professional with a passion for supporting clinical studies, apply now to join Medtronic as a Clinical Studies Support Coordinator III in Mumbai.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
Airoli | Ambernath | Amravati | Aurangabad | Dhule | Dombivali | Jalgaon | Kolhapur | Kurkumbh | Kurla | Madhapur | Mumbai | Nagpur | Nashik | Navi Mumbai | Pune | Pune city | Shirpur | Tandalja | Tarapur | Thane | Vikhroli | Yerawada |Haryana :
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Siliguri |Illinois :
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