Clinical Research Coordinator Gastroenterology
UCSF • San Francisco, CA18d • Onsite
Clinical Research Coordinator Jobs
1,503 jobs found — updated daily
Clinical/Translational Research Coordinator II
Vanderbilt University Medical Center • Nashville, TN18d • OnsiteClinical Research Coordinator
Mass General Brigham • Boston, MA18d • OnsiteClinical Research Coordinator
Prometheus Federal Services • Fairfax, VA18dSenior Clinical Research Coordinator
INNOVO RESEARCH INC • New Britain, CT18d • OnsiteCLINICAL RESEARCH COORDINATOR, SR
Duke Careers • Durham, NC18d • $69,362 - $110,658 • OnsiteClinical Research Coordinator I - Medicine
The Medical College of Wisconsin • Milwaukee, WI18d • OnsiteClinical Research Coordinator
National Institute • Victorville, CA18d • OnsiteClinical Research Coordinator II
Johnson County Clintrials LLC • Houston, TX18d • OnsiteClinical Research Coordinator
Arcetyp LLC • Seattle, WA18d • OnsiteSenior Clinical Research Coordinator
Headlands Research • Escondido, CA18d • $80,000 - $90,000 • OnsiteClinical Research Coordinator
Arcetyp LLC • San Diego, CA19d • OnsiteClinical Research Coordinator II - OBGYN
The Medical College of Wisconsin • Milwaukee, WI19d • OnsiteClinical Research Coordinator, RN
More About START • Los Angeles, CA19d • OnsiteClinical Research Coordinator I
Cedars-Sinai • Los Angeles, CA19d • $24 - $40 • OnsiteSr. Clinical Research Coordinator
Johns Hopkins University • Baltimore, MD19d • $41,300 - $72,300 • HybridClinical Research Coordinator I
Mass General Brigham • Boston, MA19d • OnsiteClinical Research Coordinator II
The Christ Hospital Health Network • Cincinnati, OH19d • OnsiteClinical Research Coordinator
Mount Sinai Health System • New York, NY19dClinical Research Coordinator IV
Emory • Atlanta, GA19d
Clinical Research Coordinator Gastroenterology
UCSF•San Francisco, CA
•Onsite
About The Position
The incumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies; 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, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or 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; and perform other duties as assigned.
Requirements
- Management and coordination of clinical research studies
- Data and specimen management
- Database and dataset management and reporting
- Coordination of staff work schedules
- Training of Assistant CRCs
- Oversight of research staff
- Management of Investigator’s protocols in the Committee on Human Research online system
- Handling renewals and modifications of protocol applications
- Implementation of new studies
- Review and writing of protocols for IRB approval
- Ensuring University compliance
- Assuring compliance with regulatory agencies
- Overseeing study data integrity
- Implementing and maintaining quality control procedures
- Interfacing with departments for UCSF approval
- Maintaining regulatory documents
- Reporting study progress to investigators
- Participating in audits and reviews
Responsibilities
- Supporting the management and coordinating the tasks of multiple clinical research studies
- Acting as intermediary between services and departments while overseeing data and specimen management
- Managing and reporting on study results
- Creating, cleaning, updating, and managing databases and comprehensive datasets and reports
- Coordinating staff work schedules
- Assisting with training of Assistant CRCs
- Assisting Clinical Research Supervisor and/or PI with oversight of other research staff
- Managing 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
- Participating in the review and writing of protocols to ensure institutional review board approval within University compliance
- Helping assure compliance with all relevant regulatory agencies
- Overseeing study data integrity
- Implementing and maintaining periodic quality control procedures
- Interfacing with departments to obtain UCSF approval prior to study initiation
- Maintaining all regulatory documents
- Reporting study progress to investigators
- Participating in any internal and external audits or reviews of study protocols
- Performing other duties as assigned
Benefits
- Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Job Search Resources
Build a Resume for Clinical Research Coordinator
The resume builder that gets results.
- Get clear feedback so you look as qualified as you are
- Align your resume with the job to get further in the process, faster
- Take the guesswork out of resume writing
