Hybrid Clinical Research Coordinator – Study Coordination

Mayo Foundation for Medical Education and Research; Rochester (MN); Hybrid; USD 34,000 - 50,000; Full time

Job summary

Mayo Clinic in Rochester, MN is seeking a Clinical Research Coordinator to support non-therapeutic and minimal risk protocol administration. This hybrid role involves coordination with the principal investigator, participant screening, enrollment, and data collection while ensuring regulatory compliance.

The ideal candidate has an HS Diploma with experience or an Associate’s degree with related clinical experience; preference for study coordinator training and clinical research exposure.

Qualifications

• HS Diploma with at least 3 years of experience or Associate's degree with at least 1 year in clinical setting.
• Associate’s in Clinical Research from an accredited institution without experience is listed.
• Bachelor's degree in any field with clinical experience is acceptable.
• Graduate or diploma from a study coordinator training program is preferred.
• One year of clinical research experience is preferred.
• Medical terminology course is preferred.

Responsibilities

• Coordinate non-therapeutic clinical research protocols with direction from the PI or supervisor.
• Screen, enroll, and recruit research participants.
• Monitor study activities and report adverse events and protocol deviations.
• Perform data collection, abstraction, and entry; assist with regulatory duties.

Skills

Clinical research experience

Regulatory compliance

Education

HS Diploma with at least 3 years of experience

Associate's degree with at least 1 year of experience

Associate’s in Clinical Research from an accredited institution

Bachelor's degree

Job description

Mayo Clinic in Rochester, MN is seeking a Clinical Research Coordinator to support non-therapeutic and minimal risk protocol administration. This hybrid role involves coordination with the principal investigator, participant screening, enrollment, and data collection while ensuring regulatory compliance.

The ideal candidate has an HS Diploma with experience or an Associate’s degree with related clinical experience; preference for study coordinator training and clinical research exposure.