Associate Clinical Research Coordinator - Cancer Center

Mayo Clinic; Jacksonville (FL); Presencial; USD 55.000 - 75.000; Jornada completa

Descripción de la vacante

Mayo Clinic Florida is seeking a Clinical Research Coordinator to coordinate non-therapeutic clinical research protocols under the direction of the principal investigator and research staff.

You will screen, enroll, and recruit participants; monitor schedules and activities; and handle data collection, regulatory duties, and communications with study sites and agencies. Some travel may be required.

Please note that visa sponsorship is not available and relocation is not offered for this role.

Responsabilidades

• Coordinate non-therapeutic clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
• Screen, enroll, and recruit research participants and monitor research activities and subject participation.
• Perform regulatory duties related to study tasks and ensure IRB/Submissions are handled properly.

Descripción del empleo

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.

Please note that visa sponsorship is not available for this role.

This role requires the candidate to work on the Mayo Clinic Florida site. Relocation is not offered for this role.