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Clinical Research Support Coordinator

University of California - San Francisco

United States, California, San Francisco

1 Daniel Burnham Court (Show on map)

Apr 07, 2026

The Clinical Research Support Coordinator plays a pivotal role in supporting clinical research activities within the HDFCCC under the guidance of the Clinical Research Support Office Director. Responsibilities encompass operational support, protocol review and monitoring, and quality control measures. It offers a unique opportunity to collaborate with diverse faculty and staff across the HDFCCC, including those in regulatory affairs, study operations, and scientific review. This role is vital for ensuring the seamless operation of clinical studies, assisting investigators, and upholding regulatory compliance. The ideal candidate thrives in a fast-paced, dynamic environment and demonstrates strong leadership abilities coupled with excellent communication skills.

Required Qualifications

Bachelor's degree in related area and/or equivalent experience/training.Minimum of 3 years of related experienceExceptional analytical / problem-solving skills to evaluate the importance and urgency of problems.Strong skills in analyzing, researching, and synthesizing large amounts of data for preparing sound and relevant proposals/analyses.Ability to multitask with demanding timeframes.Strong policy analysis techniques. Ability to analyze complex and non-routine issues requiring innovative solutions.Knowledge of common organization or research-specific and other computer application programs. Understanding of clinical research methods and operations.Strong communication and interpersonal skills to communicate effectively, both verbally and in writing.Ability to use discretion and maintain all confidentiality.Ability to operate effectively in a changing organizational and technological environment.Ability to interpret and apply policies and regulations.

Preferred Qualifications

Significant project and clinical trial management experience or progressively responsible experience in a related position, including regulatory and compliance responsibilities.Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up.

Required Qualifications :

Bachelor's degree in related area and/or equivalent experience/training.
Minimum of 3 years of related experience
Exceptional analytical / problem-solving skills to evaluate the importance and urgency of problems.
Strong skills in analyzing, researching, and synthesizing large amounts of data for preparing sound and relevant proposals/analyses.
Ability to multitask with demanding timeframes.
Strong policy analysis techniques. Ability to analyze complex and non-routine issues requiring innovative solutions.
Knowledge of common organization or research-specific and other computer application programs. Understanding of clinical research methods and operations.
Strong communication and interpersonal skills to communicate effectively, both verbally and in writing.
Ability to use discretion and maintain all confidentiality.
Ability to operate effectively in a changing organizational and technological environment.
Ability to interpret and apply policies and regulations.

Preferred Qualifications :

Significant project and clinical trial management experience or progressively responsible experience in a related position, including regulatory and compliance responsibilities.
Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up.