University of California, San Francisco
Senior Clinical Research Coordinator - GU Oncology program
University of California, San Francisco, San Francisco, California, United States, 94199
Senior Clinical Research Coordinator - GU Oncology program
University of California, San Francisco (UCSF) invites applications for a Senior Clinical Research Coordinator to support the GU Oncology program at the Helen Diller Family Comprehensive Cancer Center (HDFCCC). This full‑time, 100% position (hourly rate $41.72–$67.10) is based in the Mission Bay campus of UCSF and requires onsite work Monday‑Friday.
Job Summary
Senior Clinical Research Coordinators independently coordinate one or more clinical studies, typically a mix of NIH and industry‑sponsored multicenter trials, investigator‑initiated trials, and programmatic research activities (clinical database, biorepository). They provide leadership to lower‑level coordinators, maintain IRB compliance, negotiate contracts, oversee subject recruitment, ensure enrollment goals, and manage budgets and quality improvement processes. The role is a leadership position ensuring research commitments are met and that the program maintains a reputation for excellence.
Required Qualifications
Bachelor’s degree in a related area and sufficient experience to perform assigned duties.
Ability to develop and adjust recruitment strategies in complex environments.
In‑depth knowledge of clinical research contracts and grants, protocols, FDA regulations, and visit structures.
Project‑management skills for overseeing clinical trial operations and recruiting strategies.
Exceptional analytical, interpersonal, verbal, and written communication skills.
Ability to solve complex, non‑routine issues and adapt to a changing environment.
Experience with audit risk assessment, project planning, and motivating teams.
Interpretation and application of policies and regulations.
Financial analysis abilities, including budgeting and financial projections.
Significant clinical trial management experience with regulatory and compliance responsibilities.
Proficiency with database software such as MS Access or FileMaker Pro.
Preferred Qualifications
Fluency in spreadsheet software and ability to develop complex spreadsheets independently.
Experience in risk management for study subjects and federal/non‑federal sponsors.
Experience with grant application procedures, contract generation, and subcontracting.
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.
Licensing / Certification
Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of hire.
Location
– San Francisco, CA (Mission Bay).
Salary Range
– $41.72 – $67.10 per hour.
Equal Employment Opportunity
– The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
To learn more about UCSF and the comprehensive cancer center, visit https://www.ucsf.edu for more information.
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Job Summary
Senior Clinical Research Coordinators independently coordinate one or more clinical studies, typically a mix of NIH and industry‑sponsored multicenter trials, investigator‑initiated trials, and programmatic research activities (clinical database, biorepository). They provide leadership to lower‑level coordinators, maintain IRB compliance, negotiate contracts, oversee subject recruitment, ensure enrollment goals, and manage budgets and quality improvement processes. The role is a leadership position ensuring research commitments are met and that the program maintains a reputation for excellence.
Required Qualifications
Bachelor’s degree in a related area and sufficient experience to perform assigned duties.
Ability to develop and adjust recruitment strategies in complex environments.
In‑depth knowledge of clinical research contracts and grants, protocols, FDA regulations, and visit structures.
Project‑management skills for overseeing clinical trial operations and recruiting strategies.
Exceptional analytical, interpersonal, verbal, and written communication skills.
Ability to solve complex, non‑routine issues and adapt to a changing environment.
Experience with audit risk assessment, project planning, and motivating teams.
Interpretation and application of policies and regulations.
Financial analysis abilities, including budgeting and financial projections.
Significant clinical trial management experience with regulatory and compliance responsibilities.
Proficiency with database software such as MS Access or FileMaker Pro.
Preferred Qualifications
Fluency in spreadsheet software and ability to develop complex spreadsheets independently.
Experience in risk management for study subjects and federal/non‑federal sponsors.
Experience with grant application procedures, contract generation, and subcontracting.
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.
Licensing / Certification
Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of hire.
Location
– San Francisco, CA (Mission Bay).
Salary Range
– $41.72 – $67.10 per hour.
Equal Employment Opportunity
– The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
To learn more about UCSF and the comprehensive cancer center, visit https://www.ucsf.edu for more information.
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