Position Overview
The Clinical Research Assistant is responsible for providing support to the clinical research
coordinators (CRCs) through direct and administrative involvement in the conduct of research within the clinic. It is expected that the Research Assistant would support multiple coordinators on various clinical trial protocols. The CRA is a liaison between clinic and research staff.
Responsibilities:
- Upholds Panoramic Health Core Values
- Willing to undergo research and study specific training as necessary.
- Work under the general supervision of the Principal Investigator (PI) on sponsored research
- projects performing standard research and laboratory procedures.
- Follows Good Clinical Practices (GCPs), Panoramic Science Standard Operating Procedures (SOPs), and Study Protocol requirements regarding all procedures, laboratory activities, and data entry criteria as assigned.
- Maintains research records, source documents and related equipment, lab area and supplies in a neat professional manner
- Assists Clinical Research Coordinator(s) (CRCs) and Research Nurse(s) on study protocols by
- organizing regulatory files, data entry into the study specific edc, organizing source documentation in advance of a monitoring visit, obtaining dry ice when needed, unpacking and organizing lab kits,
- amongst other administrative duties.
- Handles incoming and outgoing calls for research such as: patient scheduling, pre-screening,
- scheduling monitoring visits.
- Performs aspects of routine research visits, such as vital signs, EKG's, medical history, and documentation
- Maintains positive relationships with research staff, clinic staff, study participants, and Sponsor/CRO staff
- Travel to other locations and to Investigator and Sponsor meetings as needed.
- Perform other duties and responsibilities as required, assigned, or requested
