Urology Trials: Clinical Research Coordinator

University of California, Davis; Sacramento (CA); Presencial; USD 50 000 - 80 000; Tempo integral

Resumo da oferta

The University of California, Davis seeks a Clinical Research Coordinator for the Department of Urologic Surgery to manage daily clinical trials, data management, regulatory duties, and direct patient contact.

Responsibilities include coordinating trials industry-sponsored and investigator-initiated, ensuring compliance with NIH, FDA, IRB, and GCP guidelines; occasional travel and overtime may be required. This 100% on-site role supports cutting-edge urologic research.

Qualificações

• High school diploma with relevant experience and duties.
• Minimum one year of experience with study subjects (patients/participants).
• Experience starting and maintaining clinical trials per NIH/FDA/IRB guidelines.
• Regulatory process and data management experience.
• Experience obtaining informed consent from participants.
• Knowledge of federal/state regulations for human subjects research; good clinical practices.
• Knowledge of anatomy and medical terminology.
• Strong organization, writing skills, and ability to multi-task.

Responsabilidades

• DATA MANAGEMENT AND COORDINATION: manage data and coordinate trial activities.
• REGULATORY SUPPORT AND ADMINISTRATION: handle regulatory submissions and compliance.
• OTHER CLINICAL TRIAL COORDINATION AND ADMINISTRATION: perform additional tasks as needed.

Conhecimentos

Clinical research coordination

Regulatory compliance

Data management

Informed consent

Good Clinical Practices

Medical terminology

Formação académica

Bachelor's degree (preferred)

Descrição da oferta de emprego

The University of California, Davis seeks a Clinical Research Coordinator for the Department of Urologic Surgery to manage daily clinical trials, data management, regulatory duties, and direct patient contact.

Responsibilities include coordinating trials industry-sponsored and investigator-initiated, ensuring compliance with NIH, FDA, IRB, and GCP guidelines; occasional travel and overtime may be required. This 100% on-site role supports cutting-edge urologic research.