Senior Clinical Research Coordinator, Liver Biorepository

UCSF Health

San Francisco (CA)

On-site

USD 110,000 - 160,000

Full time

14 days+

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Job summary

UCSF Health is seeking a Senior Clinical Research Coordinator to independently coordinate the Ibrahim El-Hefni Liver Biorepository (IELB) and related clinical studies. You will lead regulatory and operational activities, manage biospecimen collection and data, and supervise other coordinators to ensure high-quality study delivery.

Responsibilities include IRB applications, study audits, budget oversight, and cross-functional collaboration with researchers, clinicians, and external sponsors to

Qualifications

  • Bachelor’s degree required with demonstrated related experience.
  • Strong analytical skills and effective communication are essential.
  • Experience managing clinical research regulatory processes is preferred.
  • Ability to lead teams and coordinate complex studies across multiple sites.

Responsibilities

  • Oversee operations of IELB biospecimen repository and related studies.
  • Coordinate IRB/CHR applications, continuing reviews, and safety reports to ensure regulatory compliance.
  • Lead training and supervision of other coordinators and staff in the program.
  • Develop budgets, track enrollment, and monitor study performance and audits.
  • Collaborate with sponsors, researchers, and external partners to maximize sample use.
  • Prepare project documents, reports, and communications for stakeholders.

Skills

Analytical thinking
Communication
Project management
Regulatory knowledge

Education

Bachelor’s degree in related field

Tools

MS Access
FileMaker Pro

Job description

UCSF Health is seeking a Senior Clinical Research Coordinator to independently coordinate the Ibrahim El-Hefni Liver Biorepository (IELB) and related clinical studies. You will lead regulatory and operational activities, manage biospecimen collection and data, and supervise other coordinators to ensure high-quality study delivery.

Responsibilities include IRB applications, study audits, budget oversight, and cross-functional collaboration with researchers, clinicians, and external sponsors to

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