Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Clinical Research Coordinator experience within a similar setting
- Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
- Knowledge and experience of site operations and the drug development process
- Computer proficiency in use of Microsoft Word, Excel
Responsibilities
- Coordinate clinical research studies conducted by a supervising principle investigator.
- Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
- Obtains informed consent of research subjects
- Performs patient/research participant scheduling
- Collects patient/research participant history
- Performs data entry and query resolution
- Collects, processes and ships laboratory specimens
Other
- Please note this position is fully on-site at the site in Springville, Utah
- Develops strong working relationships and maintain effective communication with study team members
- Completes all protocol related training
- May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
- Effective communication
