University of California, San Francisco
Senior Clinical Research Coordinator
University of California, San Francisco, San Francisco, California, United States, 94199
Senior Clinical Research Coordinator
University of California, San Francisco
Job Summary
Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. They provide leadership to lower‑level coordinators and other support personnel, manage multi‑center clinical trials, investigator‑initiated studies, and biorepository initiatives, and ensure compliance with CHR approval, contracts, recruitment, enrollment, safety, financial oversight, and quality improvement processes.
Required Qualifications
Bachelor's degree in a related area and sufficient experience to perform the assigned duties.
Demonstrated ability to develop recruitment strategies in complex environments and identify recruitment leads.
In‑depth knowledge of clinical research contracts and grants, protocols, FDA regulations, and complex visit structures.
Project management skills to oversee the administrative operations of the clinical trials program.
Exceptional analytical, interpersonal, verbal, and written communication skills.
Ability to analyze complex issues requiring innovative solutions and to operate effectively in a changing environment.
Ability to assess audit risk, develop project plans, and motivate a team to meet deadlines.
Ability to interpret and apply policies and regulations.
Financial analysis skills, including preparing and presenting budgets.
Significant project and clinical trial management experience or progressively responsible experience in a related position with regulatory and compliance responsibilities.
Experience using database software such as MS Access or FileMaker Pro.
Preferred Qualifications
Prior experience as a research coordinator, especially in infectious diseases or clinical trials.
Basic understanding of CMV epidemiology and prevention strategies.
Proficiency in data management software and electronic data capture systems.
Advanced spreadsheet skills and audit preparation experience.
Experience in risk management for study subjects and sponsors.
Experience with grant application procedures, contract generation, and subcontracting.
Experience with the DMID‑CROMS Learning Management System.
Strong background in lab safety compliance.
License/Certification
Good Clinical Practice (GCP) Certification.
Human Subjects Protection Training.
Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of hire.
Salary Range
$41.72 – $67.10 (Hourly Rate)
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.
Location
San Francisco, CA – Parnassus Heights (SF)
Work Style
Fully On‑Site – Monday to Friday, 8:00 am to 5:00 pm.
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Job Summary
Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. They provide leadership to lower‑level coordinators and other support personnel, manage multi‑center clinical trials, investigator‑initiated studies, and biorepository initiatives, and ensure compliance with CHR approval, contracts, recruitment, enrollment, safety, financial oversight, and quality improvement processes.
Required Qualifications
Bachelor's degree in a related area and sufficient experience to perform the assigned duties.
Demonstrated ability to develop recruitment strategies in complex environments and identify recruitment leads.
In‑depth knowledge of clinical research contracts and grants, protocols, FDA regulations, and complex visit structures.
Project management skills to oversee the administrative operations of the clinical trials program.
Exceptional analytical, interpersonal, verbal, and written communication skills.
Ability to analyze complex issues requiring innovative solutions and to operate effectively in a changing environment.
Ability to assess audit risk, develop project plans, and motivate a team to meet deadlines.
Ability to interpret and apply policies and regulations.
Financial analysis skills, including preparing and presenting budgets.
Significant project and clinical trial management experience or progressively responsible experience in a related position with regulatory and compliance responsibilities.
Experience using database software such as MS Access or FileMaker Pro.
Preferred Qualifications
Prior experience as a research coordinator, especially in infectious diseases or clinical trials.
Basic understanding of CMV epidemiology and prevention strategies.
Proficiency in data management software and electronic data capture systems.
Advanced spreadsheet skills and audit preparation experience.
Experience in risk management for study subjects and sponsors.
Experience with grant application procedures, contract generation, and subcontracting.
Experience with the DMID‑CROMS Learning Management System.
Strong background in lab safety compliance.
License/Certification
Good Clinical Practice (GCP) Certification.
Human Subjects Protection Training.
Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of hire.
Salary Range
$41.72 – $67.10 (Hourly Rate)
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.
Location
San Francisco, CA – Parnassus Heights (SF)
Work Style
Fully On‑Site – Monday to Friday, 8:00 am to 5:00 pm.
#J-18808-Ljbffr