CLIN RSCH CRD
About The Position
This is a targeted posting for a Clinical Research Coordinator with experience in psychedelic research to support an NIA-funded, multisite clinical trials consortium. This role is critical to advancing the study. The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI); will coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Requirements
- Experience in psychedelic research
- Experience supporting an NIA-funded, multisite clinical trials consortium
- Ability to execute, manage, and coordinate research protocols independently or with general direction
- Ability to coordinate data collection and operations of concurrent clinical research studies
- Knowledge of research protocols, UCSF, and regulating agency policies
Responsibilities
- Support the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity.
- Act as intermediary between services and departments while overseeing data and specimen management.
- Manage and report on study results.
- Create, clean, update, and manage databases and comprehensive datasets and reports.
- Coordinate staff work schedules, recruit and train Assistant CRCs for the research team, and assist the PI with oversight of other research staff.
- Manage Investigator’s protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies.
- Participate in the review and writing of protocols to ensure institutional review board approval within University compliance.
- Help assure compliance with all relevant regulatory agencies.
- Oversee study data integrity.
- 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.
- Participate in any internal and external audits or reviews of study protocols.
- Perform other duties as assigned by the PI.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
