IMARC Research, Inc. is a Clinical Research Organization. IMARC serves as the DSMB/CEC Administrator for studies on behalf of the study sponsor. The DSMB/CEC may meet in-person and/or via web conference according to the study requirements (short and long term projects available) in order to review cumulative safety data or adjudicate adverse events. Meetings are typically held in the evenings to accommodate patient care schedules.
The DSMB provides recommendations to the study sponsor to continue, modify, or terminate the study based on their review. The CEC adjudicates adverse events and considers potential relatedness to study procedures or investigational products. Members may be asked to review and respond to safety notifications via email between meetings. Training on the study and DSMB/CEC member responsibilities will be provided. Potential members will be invited to meet or talk with a board member or chairperson, sponsor representative(s), and IMARC Research staff, prior to joining the board.
Salary commensurate with experience.
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