Clinical Research Coordinator - Physical Medicine Rehabilitation

Mayo; Rochester (MN); Híbrido; USD 39.000 - 58.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work nearby Rochester

Descripción de la vacante

Mayo Clinic in Rochester, MN seeks a clinical research coordinator to independently manage complex protocols and ensure regulatory compliance. The role involves screening, enrolling, and recruiting participants, coordinating study logistics, and providing training within the department. Travel may be required, and a hybrid on-site arrangement is offered near Rochester.

Exemption status is Nonexempt. Schedule is Full Time with 64 hours per pay period. Visa sponsorship is not available.

Formación

• HS Diploma with at least 5 years of clinical research coordination/related experience or
• Associate's degree with at least 3 years of experience or completion of Mayo Clinic internship in lieu of 1 year, as applicable
• Experience should be in a clinical research setting or related field

Responsabilidades

• Coordinate complex clinical research protocols with minimal direction in compliance with regulatory laws
• Screen, enroll, and recruit research participants; monitor subject participation and data quality
• Manage protocol development, regulatory duties, and study logistics; travel may be required

Conocimientos

Clinical research coordination

Regulatory compliance

IRB processes

Educación

HS Diploma

Associate's degree

Bachelor's degree

Clinical Research internship

Descripción del empleo

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

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.

*Please note this position is a 0.80 FTE (64 hours per pay period or every two weeks).

*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 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.

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

$27.99 - $41.98 / hour

Benefits Eligible

Yes

Schedule

Full Time

Hours/Pay Period

64

Schedule Details

Schedule varies, but will mostly be Monday through Thursday. This is a hybrid position and must be located within 100 miles of the Rochester, MN campus to work onsite. The on-site expectations will be discussed at the time of offer.

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.

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'. Mayo Clinic participates in E-Verify 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.