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Clinical Research Coordinator

University of California - San Francisco
United States, California, San Francisco
1 Daniel Burnham Court (Show on map)
Apr 07, 2026


Required Qualifications:

  • High School graduation and sufficient experience and demonstrated skills to successfully perform the assigned and responsibilities; and or an equivalent combination of education and experience.

  • Attention to detail; strong interpersonal and program management skills; excellent, effective verbal and written communication skills to coordinate with participants, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.

  • Ability to work well independently, complete projects in a timely manner, and manage multiple projects to ensure the completion of essential tasks by deadlines.

  • Experience with questionnaire design, administration, and data management

  • Prior experience in coordinating study recruitments in clinical research environments and differing participant pools and following existing strategies to meet current recruitment goals.

  • Prior experience in designing and enhancing forms for data collection, manuscripts. Demonstrate ability to develop and maintain systems for assuring protocol adherence and data quality.

Preferred Qualifications:

  • Bachelor's degree and 2 years program management experience, or an equivalent combination of education and experience.

  • Master's degree in a health or public health, research, or administration discipline.

  • Bi-cultural/bilingual in Spanish or part of the BIPOC community.

  • Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system.

  • Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation; experience with community engaged research projects

  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals

  • Experience with electronic medical records.

  • Experience with design, development, and testing of telehealth interventions

  • Familiarity with behavioral health navigators and behavioral health services

  • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms.

  • Experience applying the following regulations and guidelines:

    • Good Clinical Practice Guidelines

    • Health Information and Accountability Act (HIPAA)

    • The Protection of Human Research Subjects

    • CHR regulations for recruitment and consent of research subjects

    • Effective Cash Handling Procedures

    • Environmental Health and Safety Training

    • Fire Safety Training



Required Qualifications:

  • High School graduation and sufficient experience and demonstrated skills to successfully perform the assigned and responsibilities; and or an equivalent combination of education and experience.

  • Attention to detail; strong interpersonal and program management skills; excellent, effective verbal and written communication skills to coordinate with participants, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.

  • Ability to work well independently, complete projects in a timely manner, and manage multiple projects to ensure the completion of essential tasks by deadlines.

  • Experience with questionnaire design, administration, and data management

  • Prior experience in coordinating study recruitments in clinical research environments and differing participant pools and following existing strategies to meet current recruitment goals.

  • Prior experience in designing and enhancing forms for data collection, manuscripts. Demonstrate ability to develop and maintain systems for assuring protocol adherence and data quality.

Preferred Qualifications:

  • Bachelor's degree and 2 years program management experience, or an equivalent combination of education and experience.

  • Master's degree in a health or public health, research, or administration discipline.

  • Bi-cultural/bilingual in Spanish or part of the BIPOC community.

  • Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system.

  • Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation; experience with community engaged research projects

  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals

  • Experience with electronic medical records.

  • Experience with design, development, and testing of telehealth interventions

  • Familiarity with behavioral health navigators and behavioral health services

  • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms.

  • Experience applying the following regulations and guidelines:

    • Good Clinical Practice Guidelines

    • Health Information and Accountability Act (HIPAA)

    • The Protection of Human Research Subjects

    • CHR regulations for recruitment and consent of research subjects

    • Effective Cash Handling Procedures

    • Environmental Health and Safety Training

    • Fire Safety Training

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