Associate Clinical Research Coordinator at Mayo Clinic… · Scottsdale

Summary: Mayo Clinic Healthcare London is a renowned institution known for its commitment to research and patient care. They are seeking an Associate Clinical Research Coordinator to assist in coordinating clinical research protocols, recruiting participants, and ensuring compliance with regulatory guidelines. The role involves administrative tasks related to research studies, including data collection and protocol management. Responsibilities: - 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 - 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 - Participates in other protocol development activities and executes other assignments as warranted and assigned Required Qualifications: - 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 Preferred 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 Required Skills: Clinical Research Coordination, Regulatory Compliance, Institutional Review Board (IRB) Submission, Protocol Development, Research Data Collection, Medical Terminology