Assistant Clinical Research Coordinator - Pediatric CHAMP Program

UCSF•San Francisco, CA

22h•$33 - $54

About The Position

The overall goal of the position is to support the developing research enterprises of the Child Health Advanced Molecular Phenotyping (CHAMP) Program, which is designed to help investigators better understand childhood disease by making high-quality human biological samples and molecular data more accessible across UCSF. Many serious pediatric illnesses remain difficult to explain using traditional clinical information alone. CHAMP addresses this gap by supporting the careful collection, processing, preservation, and study of biological samples from children across a wide range of diseases and clinical settings. The goal is to make it easier for researchers to connect what is happening in a child's body at the molecular and cellular level with the clinical course of illness. CHAMP is built around two complementary goals. The first is to create a coordinated infrastructure for collecting biofluids and tissues from willing participants, especially children with severe, rare, or poorly understood diseases. Whenever possible, samples are obtained from the sites most relevant to disease and are processed using protocols designed to preserve their value for both current and future technologies. The second goal is to pair these samples with advanced molecular profiling platforms that can generate detailed information about immune responses, gene expression, cellular states, antibodies, pathogens, and other features of disease biology. These data can then be used by investigators across UCSF to generate new hypotheses, identify disease mechanisms, and ultimately improve diagnosis and treatment for children. CHAMP operates under IRB-approved protocols that allow collection of human biofluids and tissues, including biopsy and post-mortem specimens, across organ systems and age groups. The program has developed workflows for rapid processing, cryopreservation, and live cell preservation so that valuable samples can be studied with the best available technologies.

Requirements

Fully operational journey level of the series
Ability to execute, manage, and coordinate research protocols
Ability to coordinate data collection and operations of clinical research studies
Ability to manage and report on study results
Ability to create, clean, update, and manage databases and comprehensive datasets and reports
Ability to manage Investigator’s protocols in the Committee on Human Research online system
Ability to help assure compliance with all relevant regulatory agencies
Ability to oversee study data integrity
Ability to implement and maintain periodic quality control procedures
Ability to interface with departments to obtain UCSF approval prior to study initiation
Ability to maintain all regulatory documents
Ability to report study progress to investigators
Ability to participate in internal and external audits or reviews of study protocols

Responsibilities

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 two concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Support the management and coordination of the tasks of single or multiple clinical research studies, depending on their size and complexity.
Act as intermediary between services and departments while overseeing data and specimen management.
Manage and report on study results.
Create, clean, update, and manage databases and comprehensive datasets and reports.
Manage 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.
Participate in the review and writing of protocols to ensure institutional review board approval within University compliance.
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.
Perform other duties as assigned.