Clinical Studies Support Coordinator II | Medtronic – Remote (Mumbai, India)
Location: Mumbai, Maharashtra, India (Remote)
Job Type: Full-time
Experience Required: Minimum 2 years in clinical research or clinical study coordination
Industry: Medical Devices | Clinical Research | Healthcare Technology
About Medtronic
Medtronic is a global leader in healthcare technology, dedicated to innovating solutions that improve lives and expand access to quality care. Our mission—to alleviate pain, restore health, and extend life—drives a team of over 95,000 professionals worldwide who bring engineering, scientific, and clinical expertise to solve the most pressing health challenges.
At Medtronic, you’ll have the opportunity to explore, innovate, and impact global healthcare while growing in a collaborative, purpose-driven environment.
Job Overview
The Clinical Studies Support Coordinator II provides critical operational support for clinical trials, ensuring accuracy, compliance, and efficiency in data and document management. This role actively supports study execution, data integrity, and documentation to facilitate smooth clinical operations for interventional and non-interventional studies.
Key Responsibilities
Data Coordination
Support clinical study database and case report form (CRF) development and testing in line with protocol requirements.
Verify study data, manage and resolve data discrepancies, and ensure timely completion of data forms.
Assist in processing study-related compensation and resolve related discrepancies.
Document Coordination
Create, maintain, and distribute clinical study files, ensuring organization, completeness, and regulatory compliance.
Assist in audits of study files, ensuring accuracy and alignment with study protocols and SOPs.
Maintain tracking systems for clinical documents and reporting.
Operational Support & Collaboration
Act as a key individual contributor within the clinical operations team, performing administrative and clerical support with autonomy.
Communicate with internal teams and stakeholders to ensure seamless study progress.
Provide guidance and support to entry-level colleagues as needed.
Required Knowledge & Experience
Minimum 2 years of relevant clinical research or study coordination experience.
Familiarity with clinical trial operations, data management, and regulatory documentation.
Proficiency in maintaining study files, tracking systems, and clinical databases.
Strong communication, organizational, and problem-solving skills.
Ability to work remotely with moderate supervision, prioritize tasks, and meet deadlines.
Desired Skills
Understanding of clinical trial protocols, CRFs, ICDs, and study reporting.
Exposure to GCP guidelines and regulatory compliance.
Experience collaborating with cross-functional clinical teams and external vendors.
Why Join Medtronic
Work remotely in a flexible, supportive environment while contributing to life-changing healthcare innovations.
Access to a competitive salary, benefits package, and short-term incentive programs.
Opportunity to collaborate with a diverse, global team dedicated to solving critical healthcare challenges.
Grow professionally in a culture of innovation, inclusion, and continuous improvement.
Physical & Work Requirements
Remote work setup with minimal physical demands.
Role may require moderate schedule adjustments to support global study timelines.
SEO & GPT Optimization Keywords:
Clinical Studies Coordinator Jobs India, Clinical Research Coordinator Remote, Medtronic Clinical Operations Careers, Clinical Trial Data Coordinator, Clinical Study Document Management, GCP Compliant Clinical Support, Clinical Operations Jobs Mumbai
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