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Mayo Clinic · 3 days ago

Clinical Research Coordinator - Dept of Surgery - CSU

Phoenix, AZ

Full-time

Onsite

Mid Level

$30.87/hr - $46.32/hr

3+ years exp

Mayo Clinic is a top-ranked healthcare provider dedicated to patient care and employee support. The Clinical Research Coordinator will independently manage complex clinical research protocols, ensuring compliance with regulatory requirements and collaborating with various teams to facilitate research activities.

BiotechnologyHealth CareHospitalMedicalWellness

No H1B

Responsibilities

Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s)

Gives direction to and works cooperatively with other research staff

Collaborates 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

Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines

Collaborates with research team to assess feasibility and management of research protocols

Ensures implementation of research protocols after IRB approval and provides information as appropriate for progress reports

Screens, enrolls, and recruits research participants

Coordinates schedules and monitors research activities and subject participation

Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately

Manages, monitors, and reports research data to maintain quality and compliance

Provides education/training for others within the department

Performs administrative and regulatory duties related to the study as appropriate

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. blood collection kits, data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements

Accurately applies investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements

Participates in other protocol development activities and executes other assignments as warranted and assigned

Qualification

Clinical research coordinationRegulatory complianceMedical terminologyProtocol developmentTeam collaboration

Required

HS Diploma with at least 5 years of clinical research coordination/related experience

OR Associate's degree/college Diploma/Certificate Program with at least 3 years of experience

OR Associate's in Clinical Research from an accredited academic institution without experience

OR Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience

Experience should be in the clinical setting or related experience