About this role
Job title: Clinical Research Coordinator
About the Role The Clinical Research Coordinator (CRC) supports the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and other trials in urology under the supervision of the Clinical Research Supervisor. The role helps initiate study protocols after regulatory and budgetary approvals and reports study progress to the principal investigator. The CRC will support 4-5 studies involving patients with cancer and benign urologic diseases, including both active and follow-up studies as needed.
What You'll Do
- Independently maintain protocol files, data collection, and subject source records; develop project management documents and electronic data capture forms for each assigned study.
- Communicate with the Clinical Research Supervisor to ensure initiation of protocols post-regulatory and budgetary approval; report study progress to the appropriate PI.
- Support investigator in study project management to ensure compliance with CFR and ICH GCP guidelines as well as UCSF institutional policies and IRB protocols.
- Support the research team with coordinating multiple studies (approximately 4-5 studies) in cancer and benign urologic diseases, including active and follow-up work as patient complexity dictates.
What We're Looking For
- Experience in clinical research coordination and study management
- Ability to work under supervision and independently as needed
- Strong organizational skills, attention to detail, and ability to maintain accurate protocol files and data
- Knowledge of CFR and ICH GCP guidelines and UCSF IRB policies and processes
- Experience with data collection and electronic data forms