Associate Clinical Research Coordinator

Mayo Clinic • Rochester, MN

14h • Onsite

About The Position

Are you interested in a position that provides career development and growth? How about a position that is multifaceted, rewarding, and where the learning never stops? If so, then Mayo Clinic invites you to consider a life-changing career as an Associate Clinical Research Coordinator. As an Associate Clinical Research Coordinator, you will have the opportunity to work with a variety of people, from patients to care teams, enabling you to be a part of the legacy that puts the needs of the patients first. We have several Associate Clinical Research Coordinator positions available in multiple locations and departments. In this role, you could join an area such as Gastroenterology, Neurology, Radiology, Surgery, Orthopedics, Endocrinology, Cardiovascular Medicine, Psychiatry & Psychology, the Office of Clinical Trials, and many others. We have multiple schedules and shifts dependent upon position availability to fit your individual needs. Positions may vary in FTE, from supplemental to full-time. Some positions may also be temporary (less than one year) or limited tenure status (1-2 years in duration) and may have the possibility of turning into a regular position. When you apply, we will take the time to assess your qualifications and assess your preferences to determine which of our current openings would be the best match and ensure your application is reviewed by those active hiring managers. As an Associate Clinical Research Coordinator, you will : 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. This position will require candidates to work on campus and live within reasonable driving distance of the campus. To learn more about Research at Mayo Clinic, visit our website here . During the selection process you will participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview, a question will appear on your screen, and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question – Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps.

Requirements

• Must meet one of the following: 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.
• This position will require candidates to work on campus and live within reasonable driving distance of the campus.
• Visa sponsorship is not available for this position.
• This position is not eligible for F-1 OPT STEM extension.

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