Clinical Research Coordinator - Comprehensive Cancer Center
About The Position
Mayo Clinic is a top-ranked care provider, dedicated to putting patients first and investing in its employees with competitive compensation and comprehensive benefits. This role offers continuing education and advancement opportunities for a long, successful career. As a Clinical Research Coordinator, you will independently coordinate complex clinical research protocols, collaborate with the research team, ensure protocol implementation, screen and enroll participants, manage research data, provide education, and perform administrative and regulatory duties. You will also be involved in protocol development and maintenance, including document preparation, submission to IRBs, and providing consultative expertise. Some travel may be required, and this position may offer a hybrid work option after some time, requiring proximity to the Rochester, MN campus. Visa sponsorship is not available.
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.
- Ensure implementation of research protocols after IRB approval and provide information as appropriate for progress reports.
- 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.
- Perform 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. 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 apply 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.
- Participate in other protocol development activities and execute other assignments as warranted and assigned.
Benefits
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
