The Clinical Research Coordinator (CRC) serves as the project manager for assigned projects and works directly with the Research Program manager and Clinical Research Associates I & II to coordinate and implement studies.
This position will support a wide variety of research, quality improvement, and educational activities for the Pain Medicine, Palliative Care and Integrative Medicine program. Ideal candidates will have an interest in pain research, as well as experience with research activities such as writing (e.g., grant applications, manuscripts) and data management.
Responsibilities include but are not limited to the following:
Organize and manage all aspects of assigned research activities and ensure compliance with study protocols and overall clinical research objectives
Contribute methodological and technical expertise in the design, implementation, analysis and reporting of research Prepare regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
Provide support to the preparation and management of grants
Perform budget preparation and management, as needed
Facilitate and manage study-related communications (including, but not limited to communication with investigators, collaborators, regulatory bodies, and site monitors)
Proficiency with interacting with patients and families for securing informed consent, scheduling research visits, and collection of data
Oversight of data collection and entry processes
Manage personal career development and administrative tasks