
Clinical Research Coordinator - Alzheimer's Disease Research
Rochester, MN · HybridFull-time$27.99–41.98/hrSeen 6 days agoSeen in employer's feed 6 days ago
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At a glance
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Job overview
The Clinical Research Coordinator independently coordinates complex clinical research protocols, collaborating with research teams on feasibility and management. The role supports protocol implementation, participant recruitment and enrollment, research activity monitoring, adverse-event reporting, data quality, and regulatory compliance. It also includes protocol development and maintenance, IRB submissions, and consultative regulatory support. Cognitive testing is a required responsibility, with training provided for applicants without prior experience.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
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 (https://jobs.mayoclinic.org/benefits/) – 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
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Medical: Multiple plan options.
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Dental: Delta Dental or reimbursement account for flexible coverage.
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Vision: Affordable plan with national network.
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Pre-Tax Savings: HSA and FSAs for eligible expenses.
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Retirement: Competitive retirement package to secure your future.
Responsibilities
Independently coordinates 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. Collaborates with research team to assess feasibility and management of research protocols. Ensures implementation of research protocols after IRB approval and provides information as appropriate for progress reports. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately. Manages, monitors, and reports research data to maintain quality and compliance. Provides education/training for others within the department. Performs administrative and regulatory duties related to the study as appropriate. Some travel may be required. Protocol Development and Maintenance Activities Responsibilities 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. blood collection kits, data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements. Accurately applies investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements. Participates in other protocol development activities and executes other assignments as warranted and assigned.
Cognitive testing is a required part of this position. Applicants do not need prior experience but should be comfortable learning to administer standardized cognitive assessments as part of their regular responsibilities.
*Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.
Qualifications
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HS Diploma with at least 5 years of clinical research coordination/related experience OR
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Associate's degree/college Diploma/Certificate Program with at least 3 years of experience OR
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Associate's in Clinical Research from an accredited academic institution without experience OR
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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.
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Experience should be in the clinical setting or related experience.
Additional Qualifications
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Graduate or diploma from a study coordinator training program is preferred.
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One year of clinical research experience is preferred.
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Medical terminology course is preferred.
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Applicants should have a strong clinical trial background, including experience with clinical trial coordination and study conduct.
Exemption Status
Nonexempt
Compensation Detail
$27.99 - $41.98 / hour
Benefits Eligible
Yes
Schedule
Full Time
Hours/Pay Period
80
Schedule Details
Monday through Friday; This is a hybrid position and must be located within 100 miles of the Rochester, MN campus to work onsite. This hybrid work arrangement supports a combination of on-site work and offsite (remote) work according to business/department needs and will be discussed upon hire.
Weekend Schedule
Possibly work 2 to 3 Saturdays per year, dependent on Department needs.
International Assignment
No
Site Description
Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. (https://jobs.mayoclinic.org/alllocations)
Equal Opportunity
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law" (https://www.eeoc.gov/poster) . Mayo Clinic participates in E-Verify (https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf) and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization.
Recruiter
Chad Musolf
Equal opportunity
As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.
How this job compares
Set against the 641 open Clinical Research Coordinator jobs on Olive Jobs, counted November 7, 2026.
- Pay
- This posting$27.99–41.98/hr
- US median$24–36/hr201 hourly ranges
This range's midpoint, $34.99/hr, is 17% above the US median midpoint ($30/hr) — in the middle half of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 641 open Clinical Research Coordinator jobs across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Mount Sinai Health System44 open
- Actalent42 open
- Iterative Health39 open
- Experience
- This posting asks for at least 1 year of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (420 postings).
- Education
- 191 of the 641 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 7, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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