Clinical Research Coordinator: Drive Study Logistics & Data

Position Overview Coordinates non‑therapeutic (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 (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 & 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. Protocol Development and Maintenance Activities Ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (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. Participates in other protocol development activities and executes other assignments as warranted and assigned. Responsibilities Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution and works cooperatively with other investigators and personnel at all levels. Communicates with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies. 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. Qualifications Minimum Education and/or Experience Required: HS Diploma with at least 3 years of experience or Associate's degree/college Diploma/Certificate Program with at least 1 year of experience; 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 Experience and/or 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. Compensation $26.52 – $39.32 per hour; education, experience and tenure may be considered along with internal equity when job offers are extended. Schedule Full Time. Monday – Friday, 8 a.m. – 5 p.m. (location will be discussed during the interview; position will sit in either Phoenix or Scottsdale). 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. 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. Recruiter Chelsea Crosby #J-18808-Ljbffr Mayo Clinic