Part-time Clinical Research Coordinator

UCSF • San Francisco, CA

10h • Onsite

About The Position

Under the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the management of investigator-sponsored research studies as assigned/needed. Responsibilities include communicating with the Clinical Research Supervisor to ensure aspects of study initiation of protocols are developed after regulatory and budgetary approval, and report study progress to the appropriate PI. The CRC will support 4-5 research studies that are studies in patients with benign urologic diseases. This may include active and follow-up studies, depending on the complexity of the patients and procedures. Independently, the CRC maintains protocol files, data collection and subject source records, develops project management documents and electronic data forms for each assigned study. The CRC supports the investigator in research study project management to assure compliance with the Code of Federal Regulations and the ICH Guidance on Good Clinical (Research) Practice as well as UCSF Institutional policies and IRB protocols. The CRC also supports the research team with additional duties as assigned (e.g., enrolling participants, calling participants, administering surveys, etc).

Requirements

• Understanding of the Code of Federal Regulations
• Understanding of ICH Guidance on Good Clinical (Research) Practice
• Understanding of UCSF Institutional policies and IRB protocols

Responsibilities

• Support the management of investigator-sponsored research studies.
• Communicate with the Clinical Research Supervisor to ensure study initiation protocols are developed after regulatory and budgetary approval.
• Report study progress to the appropriate PI.
• Support 4-5 research studies in patients with benign urologic diseases, including active and follow-up studies.
• Maintain protocol files, data collection, and subject source records.
• Develop project management documents and electronic data forms for each assigned study.
• Support the investigator in research study project management to assure compliance with regulations and institutional policies.
• Support the research team with additional duties as assigned, such as enrolling participants, calling participants, and administering surveys.

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees