Job Details

Title: Senior Clinical Research Coordinator
Company: Stanford School of Medicine, Department of Pediatrics
Location: Palo Alto, CA (Telecommuting Possible)

The Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, is seeking a Senior Clinical Research Coordinator to perform duties related to the management and coordination of clinical studies for pediatric IBD and Celiac disease. The CRC will conduct clinical research and work independently on complex projects/assignments under the direction of multiple principal investigators. The CRC will support federal and non-federal clinical research studies including epidemiological and investigative work in support of clinical trials, clinical research or biomedical research focusing on “bench to bedside” technology.

Duties include:
• Oversee participant recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
• Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data.
• Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes.
• Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations.
• Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.
• Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.
• Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices.
• Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract.
• Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.

To Learn More & Apply:

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SOCRA Exp: 9/1/2022