Cancer Immunotherapy Clinical Research Coordinator

UCSF Health, AG

San Francisco (CA)

On-site

USD 60,000 - 90,000

Full time

14 days+

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Job summary

The Helen Diller Family Comprehensive Cancer Center at UCSF Health is seeking a Clinical Research Coordinator to join the Cancer Immunotherapy Research & Clinical Translation (CIRCT) Program within the Division of Hematology/Oncology.

The CRC will independently execute and manage protocols, coordinate data collection, and oversee study operations across sponsored, cooperative, and investigator-initiated trials.

Qualifications

  • High School Diploma or equivalent experience/training.
  • Experience in clinical research or related training in a clinical setting.
  • Familiarity with specimen processing or ability to learn in a lab environment.
  • Ability to work with oncology patients.
  • Ability to coordinate across multiple supervisors.
  • Strong attention to detail and communication skills.
  • Ability to multi-task in a fast-paced environment and meet deadlines.
  • Knowledge of research concepts and biological sciences.

Responsibilities

  • Coordinate multiple clinical studies and data management.
  • Oversee data integrity and reporting on study results.
  • Assist with regulatory documents and audits.
  • Support training of Assistant CRCs and ensure compliance.
  • Interface with departments to obtain approvals prior to study initiation.
  • Maintain databases and comprehensive datasets.

Skills

Attention to detail
Strong communication
Multi-tasking
Independent work
Team coordination

Education

High School Diploma or equivalent
Bachelor's degree in science or related

Tools

OnCore
Electronic medical records
Microsoft Office

Job description

The Helen Diller Family Comprehensive Cancer Center at UCSF Health is seeking a Clinical Research Coordinator to join the Cancer Immunotherapy Research & Clinical Translation (CIRCT) Program within the Division of Hematology/Oncology.

The CRC will independently execute and manage protocols, coordinate data collection, and oversee study operations across sponsored, cooperative, and investigator-initiated trials.

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