HCA, Hospital Corporation of America Clinical Research Coordinator in Ogden, Utah

Our northern Utah facility serves a large community with our variety of services including: a cancer treatment center, women's services, cardiology services, and an alcohol and chemical dependency treatment center as well as many others. We were listed in the Truven Health Analytics top 100 hospitals for 2013 and continue our path of excellence in healthcare. Ogden Regional is at the heart of the mountains with over six ski resorts within an hour's drive. There is also a great downtown area with restaurants and shops to satisfy all tastes. With a great university down the road and many schools within driving distance, this hospital is in a great central location to meet all your family's needs

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

The clinical research coordinator reports primarily to the Principal Investigator and department head, with associated responsibilities to the division administrator or program administrator.

  1. General Administrative Coordinates with Principal Investigator and department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures. Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training. Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with Federal regulations and sponsoring agency policies and procedures. Cooperates with facility compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office. Coordinates and facilitates monitoring and auditing visits. Collaborates with PI and institution to respond to any audit findings and implement approved recommendations. Cooperates with Main Member of NRG and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office.

  2. Protocol Preparation and Review

  3. Conduct of Research

  4. Reporting

    Current Utah RN License (in good standing) or RN Compact license preferred.

    Graduation from an accredited degree program in a clinical field such as a BSN or Physician's Assistant (PA) plus two years of healthcare experience; or completion or an allied health degree (e.g., Respiratory Therapy, Radiologic Technology, Licensed Practical Nurse) or Associates degree in Clinical Trials Research related curriculum plus a minimum of five years healthcare, clinical and/or research experience; or Completion of a bachelor's degree in a field related to health science plus a minimum of three years closely related clinical and/or research experience

Job: *Supervisors Team Leaders & Coordinators

Title: Clinical Research Coordinator

Location: Utah-Ogden-Ogden Regional Medical Center

Requisition ID: 06030-40377