Top Medical Research Jobs in the US – Life Science Jobs at Medtronic
Medtronic is inviting applications for the position of Medical Science Clinical Research Specialist in Cardiac Rhythm Management (CRM) at its Mounds View, Minnesota office. This full-time role offers biomedical science graduates an exceptional opportunity to combine strategic thinking with clinical research in one of the most innovative healthcare companies. With a global footprint and a commitment to patient-centric technology, Medtronic offers a dynamic role for candidates ready to impact lives.
About the Company:
Medtronic is one of the world’s largest medical technology companies, with a mission to alleviate pain, restore health, and extend life. With a global workforce of over 95,000 employees, Medtronic offers innovative healthcare solutions in more than 150 countries. The company emphasizes diversity, equity, and inclusion, fostering a work culture rooted in purpose and patient-first innovation. Medtronic is committed to employee growth through flexible benefits, structured career paths, and global collaboration.
Job Details:
Job Opening: Medical Science Clinical Research Specialist – Cardiac Rhythm Management
Location: Mounds View, Minnesota, United States of America
Time Type: Full-time
End Date to Apply: July 21, 2025
Job Requisition ID: R31854
About the Role
We are looking for a dedicated individual to join our Cardiac Rhythm Management team as a Clinical Research Specialist. In this role, you will be instrumental in advancing critical medical science initiatives and external research within our integrated operating unit. If you have a passion for strategic and operational activities in the healthcare industry, this position offers a unique opportunity to make a real impact.
Key Responsibilities Include:
-
Review and assess the External Research Program (ERP) and medical science proposals for feasibility and safety.
-
Support the decision-making process by synthesizing feedback and documenting results.
-
Conduct routine portfolio assessments and provide study-specific recommendations.
-
Coordinate each step of the board review process, ensuring regulatory and strategic compliance.
-
Collaborate cross-functionally with other Operating Units (OUs), scientists, and stakeholders.
-
Handle amendments, contract changes, and quality check action items.
-
Maintain global awareness of scientific and regulatory frameworks in clinical studies.
Qualifications:
-
Bachelor’s degree in biological sciences or biomedical engineering + 2 years clinical research experience OR
-
Master’s degree in biological sciences/biomedical engineering with 0 years of experience.
-
Strong communication, documentation, and problem-solving skills.
-
Prior experience in clinical cardiac settings is preferred.
