Under the supervision of a Clinical Research Supervisor, Project Manager, or Principal Investigator (PI), the Clinical Research Coordinator (CRC) will perform entry-level duties related to the support and coordination of clinical studies and may receive training and development to prepare and advance to the next level within the series.

The ACRC may be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials, which may include, but is not limited to, the following tasks:
* Help prepare protocols for study initiation,
* Help design flow sheets, data forms and source documents,
* Gather and interpret medical, surgical and laboratory data regarding clinical trial subjects,
* May apply understanding of inclusion/exclusion eligibility criteria for protocols,
* Help recruit, enroll, register, schedule and retain study subjects,
* Record protocol specific treatments and assure timely collection and shipment of samples,
* Assist research personnel to keep patients on study schedules,
* Complete study forms to submit to sponsors and/or appropriate agencies,
* Collect, enter and clean data into study databases, maintaining data quality,
* Assist with data analysis and preparation of reports and tables,
* Attend team and project meetings as needed,
* Perform other duties as assigned.

The final salary and offer components are subject to additional approvals based on UC policy.

Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

The salary range for this position is $28.48 - $45.80 (Hourly Rate).

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html