Clinical Research Coordinator (Osher Center)

UCSF•San Francisco, CA

About The Position

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); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF, and regulating agency policies. This position will primarily support Dr. Felder’s research focused on maternal sleep, mood, parent-child interaction, and child social-emotional outcomes. The employee’s main responsibilities pertain to study implementation, including: implementing study protocols; modifying and managing IRB applications; managing databases and conducting data quality control; distributing survey materials on REDCap; recruiting, enrolling, and retaining study participants; conducting clinical interviews with research participants; conducting experimental tasks with mothers and children; recording study data in REDCap according to good clinical practice; building and/or modifying REDCap database and reports; tracking data collection; coordinating staff work schedules; assisting with training and oversight of other staff and volunteers; assuring compliance with all relevant regulatory agencies; overseeing study data integrity; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing other duties as assigned. The employee must be able and willing to adhere to study guidelines, keep accurate records, maintain confidentiality, and attend regular study team meetings. The UCSF Osher Center for Integrative Health is an interdisciplinary center that includes clinical, educational, and research programs. Of particular relevance for this position, the UCSF Osher Center is committed to advancing the science of integrative health by conducting and disseminating rigorous research.

Requirements

Ability to perform independently or with general direction at the fully operational journey level of the series
Ability to execute, manage, and coordinate research protocols
Ability to coordinate data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF, and regulating agency policies
Ability to implement study protocols
Ability to modify and manage IRB applications
Ability to manage databases and conduct data quality control
Ability to distribute survey materials on REDCap
Ability to recruit, enroll, and retain study participants
Ability to conduct clinical interviews with research participants
Ability to conduct experimental tasks with mothers and children
Ability to record study data in REDCap according to good clinical practice
Ability to build and/or modify REDCap database and reports
Ability to track data collection
Ability to coordinate staff work schedules
Ability to assist with training and oversight of other staff and volunteers
Ability to assure compliance with all relevant regulatory agencies
Ability to oversee study data integrity
Ability to report study progress to investigators
Ability to participate in any internal and external audits or reviews of study protocols
Ability to adhere to study guidelines
Ability to keep accurate records
Ability to maintain confidentiality
Ability to attend regular study team meetings