Registered Nurse - Clinical Research Nurse (CRN)

Carenest Health Services•Santa Monica, CA

5d•Hybrid

About The Position

This is a full-time, temporary-to-permanent clinical research position in Santa Monica, with the possibility of hybrid work. The Clinical Research Coordinator/Senior CRC supports investigators conducting multiple clinical research trials in accordance with research center SOPs and applicable local, state, and federal regulations. In collaboration with other team members, the role coordinates enrollment, study visits, and follow-up care for patients participating in clinical trials across various therapeutic areas. The position serves as a liaison among sponsors and monitors, regulatory agencies, patients, investigators, nurses, and other staff, and participates in internal and external quality audits. The position is scheduled for five 8-hour day shifts. Candidates should be aware that the permanent rate is approximately $45–$46 per hour before accepting the contract. Living near Santa Monica is preferred because of the commute, with a preferred commute of 30 minutes or less. The role requires patient-facing clinical trial experience; device trial experience and solely data-trial experience are not accepted.

Requirements

At least 5 years of experience in a clinical research setting where the candidate managed patients.
Patient-facing clinical trial experience is required.
EPIC experience is required.
Must have a blood draw certification; the candidate must be a phlebotomist, medical assistant, LVN, or RN.
Strong computer skills, including Outlook, MS Teams, Word, and Excel.
Device trial experience is not accepted; solely data-trial experience is also not accepted.
Must be aware of the approximate permanent rate of $45–$46 per hour before accepting the contract.

Nice To Haves

CCRC certification through ACRP is preferred.
Experience with neurological conditions is a plus.
Spanish or Korean language skills are a plus.
Living in or near Santa Monica is preferred, with a commute of 30 minutes or less preferred.
Hybrid work may be available if preferred.

Responsibilities

Support investigators in conducting multiple clinical research trials in accordance with research center SOPs and applicable local, state, and federal regulations.
Coordinate enrollment, study visits, and follow-up care for patients participating in clinical trials.
Serve as a liaison among sponsors and monitors, regulatory agencies, patients, investigators, nurses, and other staff during trials.
Participate in internal and external quality audits.
Perform job functions in a timely and efficient manner.
Act as the primary CRC for more complex protocols or patient populations.
Consistently exceed the minimum CRC workload index.
Assist in training new research assistants and CRCs as needed.
Follow the organization’s Code of Conduct, mission, vision, shared values, policies, procedures, standards, and practices.
Promptly report suspected or potential violations and cooperate in investigations.
Maintain professional appearance and conduct, good rapport and cooperative working relationships with staff and physicians, and organizational and patient confidentiality.
Represent the organization positively and professionally in the community.
Maintain excellent attendance.