Associate Clinical Research Coordinator - Cbru

Community Based Research Unit

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. ADDENDUM (if applicable) 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. 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.

HS Diploma with at least 3 years' experience in the clinical setting or related experience including competency in Outlook, Excel, and Epic OR Associates degree or completion of a college Diploma or Certificate Program with at least 1-year experience in the clinical setting or related experience including competency in Outlook, Excel, and Epic OR Bachelor's degree, healthcare or science related field preferred.
Graduate or diploma from a study coordinator training program is preferred. One year clinical research experience preferred. Medical terminology course preferred.

Preference given to candidates with the following qualifications:

• Ability to work onsite at the Mayo Clinic main campus (4500 San Pablo Road, Jacksonville FL 32224) and downtown at the Mayo Clinic Community Health Collaborative (214 N Hogan St, Jacksonville, FL 32202),
• Bilingual English & Spanish
• Sincere interest in promoting research within local underrepresented communities.
• Phlebotomy Certification

Visa sponsorship is not available for this position. Mayo does not participate in the OPT STEM program.