Clinical Research Coordinator HEMOC
About The Position
The Clinical Research Coordinator (CRC) will work with a close-knit group of health services researchers and clinicians at the University of California, San Francisco and San Francisco VA Health Care System, who are focused on improving the health of older persons. We are looking for a highly motivated candidate with a strong work ethic who has a background in clinical research or a related field, to assist the Principal Investigator (PI) on a study related to health services. The CRC 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 Clinical Research Supervisor and/or Principal Investigator (PI); coordinate the data collection and operations of clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Requirements
- Background in clinical research or a related field
- Strong work ethic
- Highly motivated
Responsibilities
- Recruiting research subjects (identification, determine eligibility and obtain consent of potential research participants)
- Obtaining medical and health information from participants and abstracting information from electronic clinical records
- Administering surveys
- Conducting semi-structured interviews
- Overseeing participant payments
- Creating, cleaning, updating, and managing qualitative and quantitative datasets and reports
- Analyzing data using quantitative and qualitative methods
- Assisting in conducting literature reviews
- Participate in manuscript preparation and research result presentation
- Coordinating project schedules and team meetings
- 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
- Maintaining all regulatory documents
- Participating in any internal and external audits or reviews of study protocols
- Performing other research-related duties as assigned
Benefits
- Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
