Director, Clinical Research Operations
Provides leadership, guidance, technical oversight, and regulatory support to faculty, administrators, and staff on a wide range of issues and projects for the administrative lifecycle of research studies within Norris Cotton Cancer Center, Clinical Research Office.
Bachelor’s degree in clinical science field.
Clinical Research Professional Certification preferred
Seven (7) years of relevant experience in a Clinical Research environment with three (3) years of clinical study operations management and supervisory experience required.
The Office of Clinical Research (OCR) is the established office within the Norris Cotton Cancer Center (NCCC) which supports clinical cancer research at Dartmouth. The OCR provides support for investigator-initiated trials (IIT), cooperative group trials (as an NCTN Lead Academic Participating Site [LAPS], NCI ETCTN, and Full Member of Alliance, NRG, and ECOG-ACRIN), and corporate-sponsored studies. The OCR is a service group within NCCC to provide investigators centralized support and study data management, as well as protocol development, support for monitoring for cooperative group studies, screening for potential research participants, and liaison with federal and industry sponsors and regulatory bodies. The OCR provides resource support to the NCCC clinical protocol scientific review committee (known locally as the Clinical Cancer Review Committee [CCRC]), the Quality Improvement Committee, the Clinical Trial Investigational Order Set Committee (CTIOSC), and the Data Safety Monitoring and Accrual Committee (DSMAC).