Mayo Clinic
Mayo Clinic
Posted 2 days ago
Full Time
Phoenix, Arizona
In Person
Smart Summary
Responsibilities
The coordinator manages non-therapeutic clinical research protocols, including screening and enrolling participants while ensuring compliance with regulatory laws. They also handle data collection, administrative duties, and communication with investigators and institutional review boards.
Qualifications
You have a high school diploma with at least 3 years of clinical research experience, or an Associate's degree with at least 1 year of experience, or a Bachelor's degree. Experience in a clinical setting or related field is required, and a study coordinator training program, clinical research experience, and medical terminology courses are preferred.
Must Have Skills for ATS
Clinical Research
Medical Terminology
IRB Submission
Data Collection
Protocol Development
Job Description
Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.
Position Overview: (Major Functions and Non-Essential Functions):
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.
This position is not eligible for visa sponsorship. Please note that Mayo Clinic does not participate in the OPT Stem Program.
Mayo Clinic
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