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Associate Clinical Research Coordinator - Gastroenterology and Hepatology - Limited Tenure

Job in Rochester, Olmsted County, Minnesota, 55905, USA
Listing for: Mayo Clinic
Full Time position
Listed on 2026-01-27
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 24.07 - 34.95 USD Hourly USD 24.07 34.95 HOUR
Job Description & How to Apply Below

Overview

Why Mayo Clinic
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.

Why Mayo Clinic
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.

Benefits

Highlights
  • Medical:
    Multiple plan options.
  • Dental:
    Delta Dental or reimbursement account for flexible coverage.
  • Vision:
    Affordable plan with national network.
  • Pre-Tax Savings: HSA and FSAs for eligible expenses.
  • Retirement:
    Competitive retirement package to secure your future.
Responsibilities

As an Associate Clinical Research Coordinator, you:

  • 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 (i.e. interventional, therapeutic, greater than minimal risk) 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 report appropriately.
  • Collect, abstract, and enter research data.
  • Perform administrative and regulatory duties related to the study as assigned.
  • May be required to do some travel.
  • Participate in Protocol Development and Maintenance Activities Responsibilities, which may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards;
    Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes.
  • Participate in other protocol development activities and execute other assignments as warranted and assigned.
Selection Process

During the selection process you may 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.

  • This is a limited tenure position with an anticipated duration of up to two years, that may have the possibility of turning into a regular status position.
  • Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.
Qualifications
  • 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.
Additional Qualifications
  • Graduate or diploma from a study coordinator training program is preferred.
  • One year of clinical research experience is preferred.
  • Medical terminology course is preferred.
Exemption Status

Nonexempt

Compensation Detail

$24.07 - $34.95 / hour

Benefits Eligible

Yes

Schedule

Full Time

Hours/Pay…
Position Requirements
10+ Years work experience
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