About this role
Job title: Clinical Research Coordinator
Join UCSF's Department of Emergency Medicine as a Clinical Research Coordinator responsible for coordinating multiple clinical studies. This role acts as an intermediary among services and departments, overseeing data and specimen management, and supporting the design, approval, and execution of research protocols in alignment with university compliance and regulatory requirements.
What You'll Do
- Coordinate the tasks of multiple clinical research studies within the Department of Emergency Medicine.
- Oversee data and specimen management, and manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports.
- Train research volunteers; coordinate all protocol applications and implementation of new studies.
- Participate in the review and writing of protocols to ensure IRB approval within University compliance; help assure compliance with all relevant regulatory agencies.
- Oversee study data integrity and implement and maintain periodic quality control procedures.
- Interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents.
- Report study progress to investigators and participate in any internal and external audits or reviews of study protocols.
- Perform other duties as assigned.
What We're Looking For
- Experience coordinating clinical research studies in a hospital or academic setting.
- Proficiency in data management, database maintenance, and reporting.
- Knowledge of regulatory requirements, IRB processes, and study approvals.
- Experience ensuring data integrity and participating in audits or reviews.
- Strong communication, organizational, and interdepartmental liaison skills; ability to train volunteers.
- Ability to initiate new studies and coordinate protocol applications.