Clinical Research Coordinator

Mayo Clinic•Rochester, MN

1d•Onsite

About The Position

Mayo Clinic is seeking a Clinical Research Coordinator for a multifaceted and rewarding position that offers career development and growth. This role involves working with patients and care teams, contributing to a legacy of patient-first care. There are multiple positions available across various locations and departments, with flexible schedules and shifts. Positions may range from supplemental to full-time, and some may be temporary (less than one year) or limited tenure (1-2 years) with the potential to become regular positions. Applicants' qualifications and preferences will be assessed to match them with suitable openings. The role requires candidates to work on campus and be within reasonable driving distance.

Requirements

HS Diploma with at least 5 years of clinical research coordination/related experience OR Associate's degree/college Diploma/Certificate Program with at least 3 years of experience OR Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience.
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

Independently coordinate complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
Collaborate with research team to assess feasibility and management of research protocols.
Screen, enroll, and recruit research participants.
Coordinate schedules and monitor research activities and subject participation.
Identify, review, and report adverse events, protocol deviations, and other unanticipated problems appropriately.
Manage, monitor, and report research data to maintain quality and compliance.
Provide education/training for others within the department.
Perform administrative and regulatory duties related to the study as appropriate.
Participate in other protocol development activities and other assignments as assigned.
Actively partner with team members by fostering an inclusive work environment and respecting others with different backgrounds, experiences and perspectives.