Assistant Clinical Research Coordinator

UCSFSan Francisco, CA

About The Position

Under the supervision of the Principal Investigator (PI), incumbent will perform entry level duties related to support and coordination of clinical research studies evaluating evidence-based interventions for traditionally underserved populations worldwide. This is an opportunity to be a key member of an international clinical intervention research team, learn about the implementation and evaluation of a school-based mental health intervention for youth with inattention and disruptive behavior, collaborate (virtually) with researchers and community members in Mexico, and coordinate a National Institute of Health (NIH)-funded global health clinical research protocol.

Requirements

  • Entry level duties related to support and coordination of clinical research studies
  • Evaluating evidence-based interventions for traditionally underserved populations worldwide
  • Understanding of inclusion/exclusion eligibility criteria for protocols
  • Ability to recruit, enroll, register, schedule and retain study subjects
  • Ability to assist research personnel to keep subjects on study schedules
  • Ability to complete study forms to submit to sponsors and/or appropriate agencies
  • Ability to collect, enter and clean data into study databases, maintaining data quality
  • Ability to assist with data analysis
  • Ability to assist with preparation of reports and tables
  • Ability to attend team meetings
  • Ability to assist with management of study website

Nice To Haves

  • Experience with school-based mental health intervention for youth with inattention and disruptive behavior
  • Experience collaborating virtually with researchers and community members in Mexico
  • Experience coordinating NIH-funded global health clinical research protocols

Responsibilities

  • Help prepare protocols for the study
  • Help design flow sheets, data forms and source documents
  • Gather data regarding clinical trial subjects
  • May apply understanding of inclusion/exclusion eligibility criteria for protocols
  • Help recruit, enroll, register, schedule and retain study subjects
  • Assist research personnel to keep subjects 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
  • Assist with preparation of reports and tables
  • Attend team meetings
  • Assist with management of study website
  • Perform other duties as assigned

Benefits

  • Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service