Clinical Research Coordinator at UCSF

San Francisco, California, United States -

Full Time

Start Date

Immediate

Expiry Date

31 Jul, 26

Salary

38.23

Posted On

02 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research coordination, Protocol management, Data collection, Phlebotomy, Regulatory compliance, Database management, Patient recruitment, Informed consent, Quality control, IRB submission, Electronic medical records, Communication skills, Multi-tasking, Data integrity, Spanish fluency

Industry

Hospitals and Health Care

Description

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 Clinical Research Supervisor, Associate Project Director, and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. The Clinical Research Coordinator will independently execute, manage, and coordinate multiple clinical research protocols within the MACS/WIHS Combined Cohort Study (MWCCS) - a collaborative, multi-center, longitudinal study designed to comprehensively investigate the impact of chronic health conditions that affect people with HIV. CRC duties may include, but will not be limited to recruiting and screening new enrollees, supporting the management and coordinating the tasks of multiple concurrent clinical research studies; act as intermediary between services and departments while overseeing data and specimen collection; clean and update, databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of new CRCs; may assist with management of Investigator’s protocols in the Investigational Review Board online system, as well as renewals and modifications of protocol applications and the implementation of new studies; 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.

Responsibilities

The Clinical Research Coordinator will independently execute and manage multiple clinical research protocols, including participant recruitment, data collection, and specimen management. They will also ensure regulatory compliance, maintain study databases, and coordinate staff activities to support the study's objectives.