Associate Clinical Research Coordinator

Mayo Clinic • Rochester, MN

2d • Onsite

About The Position

Mayo Clinic is seeking an Associate Clinical Research Coordinator for a multifaceted and rewarding position with career development and growth opportunities. This role involves working with patients and care teams, contributing to the legacy of patient-first care. Multiple positions are available across various locations and departments such as Gastroenterology, Neurology, Radiology, Surgery, Orthopedics, Endocrinology, Cardiovascular Medicine, Psychiatry & Psychology, and the Office of Clinical Trials. The roles offer various schedules and shifts, with FTEs ranging from supplemental to full-time. Some positions may be temporary (less than one year) or limited tenure (1-2 years) with the possibility of becoming regular positions. The selection process includes an OnDemand (pre-recorded) interview. This position requires candidates to work on campus and be within reasonable driving distance.

Requirements

• HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate Program with at least 1 year of experience OR Associate’s in Clinical Research from an accredited academic institution without experience OR Bachelor's degree.
• Experience should be in the clinical setting or related experience.

Nice To Haves

• 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 (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
• May assist in complex studies with direction but does not have overall responsibility for these studies.
• Screen, enroll, and recruit research participants.
• Coordinate schedules and monitor research activities and subject participation.
• Recognize adverse events, protocol deviations, and other unanticipated problems and reports appropriately.
• Collect, abstract, and enter research data.
• Perform administrative and regulatory duties related to the study as assigned.
• Participate in other protocol development activities and executes other assignments as warranted and assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees