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Responsibilities Assist in regulatory document preparation for study Assist with the screening, recruiting, and gathering consent from study participants according to study protocol Contact and schedule participants for research studies and serve as primary contact from study start-up to closeout Collect MRI, TMS, EEG, and other psychophysiological data for clinical research projects Manage patient and laboratory dat

Cancer Clinical Research Coordinator 2 - Neurology (Hybrid) jobs in United States Tags 25 applicants Original Job Post Stanford University School of Medicine Cancer Clinical Research Coordinator 2 - Neurology (Hybrid) 82 GOOD MATCH Experience Level 100 Skill 68 Industry Exp. 76 Responsibilities Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research par

Responsibilities Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies Coordinate collection of study specimens and processing Collect and manage patient and laboratory data for clinical research proje

Stanford University’s Department of Neurosurgery seeks a Clinical Research Coordinator II to independently coordinate and oversee clinical research studies involving pediatric and adult neuro-oncology treatments. The role manages study operations, data and regulatory compliance, and supervises and trains research staff. Tags Health Care Biotechnology Healthcare Medical Insider Connection @Stanford University School o

Cancer Clinical Research Coordinator Associate – Head and Neck Surgery (Hybrid) jobs in United States Tags 25 applicants Original Job Post Stanford University School of Medicine 91 STRONG MATCH Experience Level 100 Skill 93 Industry Exp. 76 Health Care Responsibilities Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout Determine el

Responsibilities Lead subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining p articipants in long-term clinical trials Oversee and contribute to data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data Collaborate on project sche

Responsibilities Independently develop, draft and compile research protocol documents and all materials required for regulatory submissions in compliance with University and external policies Manage and oversee new study initiation process, including educating study staff and sponsors, resolving issues and providing regulatory guidance and support Facilitate and participate in committee meetings, ensure procedures ar