Providence is seeking a Clinical Research Analyst for a remote position within the HRPP. The analyst will process full-board and expedited reviews, adverse events, protocol modifications, and informed consent forms, serving as an IRB expert and liaison to researchers to ensure compliance with regulations.
This intermediate/journey-level role requires solid IRB and regulatory experience, with a focus on supporting IRB members and coordinating staff activities within the health system.
#J-18808-LjbffrRemote IRB & Regulatory Research Analyst in portland at Unknown Company
This position is listed as full time and able to be worked remotely.