Clinical Research Coordinator
Oversees, coordinates, develops, and manages the day-to-day clinical activities for specified research trials in accordance with the research parameters established by the Principle Investigator (PI). The Clinical Research Coordinator (CRC) promotes good clinical practices in the conduct of investigations by possessing an in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The CRC conducts clinical tasks per protocol and as delegated by the PI and sponsoring organizations. The CRC assures compliance with protocol and regulatory requirements, by collecting, recording, and maintaining data and source documentation. The CRC will work closely with the PI’s, department members, study sponsors, and the institution, to support administration of the compliance, financial, personnel and other related aspects of all ongoing clinical studies.
Facilitate and coordinate daily clinical activities; the position plays a critical role in the conduct of all studies.
Act as liaison between PI’s, ancillary departments, research subjects, sponsoring organizations and regulating bodies, vendors, brokers, and suppliers of products and services.
Provides technical guidance regarding interpretation of state, federal benefits legislation, ensures organizational compliance, and submits regulatory reports as required.
With program participants; conduct interviews, schedule participant appointments, administer surveys for research purposes, collect and aggregate data, and act as patient liaison for the PI.
Serve as a member of the research team.
Maintains required documentation including source documentation, subject logs, various records, reports, and other essential documents.
Data mining and data entry.
Develops contingency plans and responds to unforeseen circumstances utilizing planned resources.
Adheres to TMCH organizational and department-specific safety, confidentiality, values, policies and standards.
Performs related duties as assigned.
EDUCATION: Bachelor's degree from four-year college or university specializing in law, biomedical sciences, ethics, public health or related field; or any equivalent combination of experience, training and/or education approved by Human Resources.
EXPEREINCE: Bachelor's degree in a field appropriate to the area of assignment AND two years related research experience; OR, six years research experience appropriate to the area of assignment; OR, any equivalent combination of experience, training and/or education approved by Human Resources.
LICENSURE OR CERTIFICATION: Current Cardio Pulmonary Resuscitation (CPR) required. Accredited Clinical Research Professional or LPN licensure permitting work in the State of Arizona preferred.
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Job Status: Full Time
Job Reference #: 30299