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Protocol Project Coordinator

University of California San Francisco

Details

Posted: 22-Aug-24

Location: San Francisco, California

Type: Full-time

Salary: Open

Internal Number: 80513BR

The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is a national leader in oncology research. The HDFCCC clinical research program is a fast paced program with a broad portfolio of clinical trials. The mission of the UCSF HDFCCC clinical research program is to provide patients and their families with streamlined access to cutting-edge cancer therapies in addition to providing compassionate, patient-centered care. Our team of clinicians and researchers is dedicated to improving outcomes for all patients.

The Pediatric Oncology program is seeking a Protocol Project Coordinator with an interest in providing regulatory support to our growing program.

Under the general direction of the Program Leaders, the Protocol Project Coordinator will provide regulatory administration, project management, and administrative support for the Pediatric Oncology Research Department at the University of California San Francisco. The incumbent's responsibilities will include: interfacing with Program Investigators and study sponsors, administrative support of clinical trials, regulatory maintenance, and IRB submission tasks for clinical trial protocols.

Incumbent's duties may include, but will not be limited to, assisting with the regulatory aspects of multiple clinical research studies (sponsored, cooperative group, and investigator-initiated studies),help assure compliance with all relevant regulatory agencies implement and maintain periodic quality control procedures; ensure policies mandated by the HDFCCC, federal government, any outside entity and study team are followed during trial maintenance phase and close-out, coordinate and prepare for sponsor or collaborator visits such as site initiation, audit and monitor visits, interface with departments to assist with obtaining UCSF approval prior to study initiation; maintain relevant regulatory documents; report study progress to investigators and sponsors, update clinical trial management databases, and perform other duties as assigned.

The final salary and offer components are subject to additional approvals based on UC policy.

Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

The salary range for this position is $34.32 - $55.19 (Hourly Rate).

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

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About University of California San Francisco

The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and high-quality patient care. It is the only UC campus in the 10-campus system dedicated exclusively to the health sciences.

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