Clinical Research Spec
Medtronic · Mounds View, MN
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Role summary
Clinical Research Specialist position at Medtronic's Interventional Cardiology unit in Mounds View, Minnesota, focusing on study execution and site management for cardiovascular device clinical programs. Role involves regulatory compliance, site coordination, data integrity oversight, and cross-functional collaboration to advance device-based technologies.
What they're looking for
- Bachelor's degree and minimum 2 years clinical research experience, or advanced degree
- Experience in clinical study site management and protocol compliance
- Knowledge of Good Clinical Practice (GCP) and regulatory standards for clinical trials
- CCRA or SOCRA certification preferred
- Medical device industry or clinical research experience preferred
- Project management and multi-site study execution skills
What you'll be doing
- Manage study initiation, site activation, and closure activities for clinical programs
- Coordinate with clinical sites to ensure protocol compliance, data integrity, and regulatory adherence
- Review and approve study documentation, maintain site files, and track regulatory requirements
- Perform data review, identify discrepancies, and ensure resolution of monitoring action items
- Support clinical management with protocol development, case report forms, and progress reporting
Privacy & handoff
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