Associate Clinical Research Coordinator - Comprehensive Cancer Center
About The Position
Mayo Clinic is a top-ranked healthcare provider dedicated to patient needs and employee well-being. They offer competitive compensation, comprehensive benefits, and opportunities for continuing education and career advancement. This role involves coordinating clinical research protocols, screening and enrolling participants, monitoring study activities, and managing data. The position may also involve protocol development, IRB submissions, and communication with study sites and federal agencies. The selection process may include an OnDemand interview. Visa sponsorship is not available.
Requirements
- 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.
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
- Coordinates 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.
- Screens, enrolls, and recruits research participants.
- Coordinates schedules and monitors research activities and subject participation.
- Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately.
- Collects, abstracts, and enters research data.
- Performs administrative and regulatory duties related to the study as assigned.
- Some travel may be required.
- 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.
- Communication with study sites and/or federal agencies regarding study status changes.
- Participates in other protocol development activities and executes 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
Entry Level
Education Level
Associate degree
