Senior Clinical Research Coordinator, GU Oncology Trials

Oncology Voice Network LLC

San Francisco (CA)

Hybrid

USD 120,000 - 160,000

Full time

14 days+

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Job summary

University of California, San Francisco is seeking a Senior Clinical Research Coordinator for the Genitourinary Medical Oncology Program in San Francisco. The role coordinates complex clinical studies, ensures CHR compliance, and provides leadership to a team across multiple trials, including IITs and multicenter collaborations.

You will manage study activation, regulatory submissions, and budgeting while maintaining high standards for safety and data integrity in a dynamic, collaborative

Qualifications

  • BS/BA degree in a related area; experience may substitute.
  • Demonstrated ability to develop recruitment strategies in complex environments.
  • In-depth knowledge of clinical research contracts and grants, trials, FDA regulations, visit structures.
  • Project management skills to oversee administrative operations of trials.

Responsibilities

  • Coordinate administrative operations of one or more clinical studies across networks.
  • Lead activation, amendments, and IIT oversight with subsites.
  • Ensure CHR approval, contract generation, and budgets; oversee enrollment and feasibility.
  • Apply quality improvement processes to improve efficiency, safety, and compliance.

Skills

Recruitment strategies
Clinical research contracts
Project management
Analytical skills
Communication skills
Audit risk assessment
Regulatory compliance

Education

BS/BA degree in a related area
Certification: SoCRA/ACRP (within 1 year)

Tools

MS Access
FileMaker Pro

Job description

University of California, San Francisco is seeking a Senior Clinical Research Coordinator for the Genitourinary Medical Oncology Program in San Francisco. The role coordinates complex clinical studies, ensures CHR compliance, and provides leadership to a team across multiple trials, including IITs and multicenter collaborations.

You will manage study activation, regulatory submissions, and budgeting while maintaining high standards for safety and data integrity in a dynamic, collaborative

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