University of California - San Francisco Campus and Health
Clinical Research Supervisor - Cutaneous Oncology Program
University of California - San Francisco Campus and Health, San Francisco, California, United States, 94199
Clinical Research Supervisor - Cutaneous Oncology Program
Full Time
Overview The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) Supervisor for the Cutaneous Oncology Program. Under the supervision of the Clinical Research Manager (CRM), the CRC Supervisor will manage and facilitate the day‑to‑day operations of a team of three to six CRCs, ensuring training, performance evaluation, data collection, protocol implementation, and compliance with federal, state, and institutional policies.
Responsibilities
Supervise and train a team of 3–6 CRCs, providing mentorship and performance evaluation.
Oversee day‑to‑day operations of assigned clinical trials, ensuring compliance with Good Clinical Practice and regulations.
Assist the CRM with operational, workload, and protocol implementation issues.
Coordinate study activation, maintenance, and submission of data and adverse event reports.
Develop and implement standard operating procedures to improve efficiency and productivity while safeguarding patient care and data integrity.
Collaborate with cross‑functional teams and maintain relationships with stakeholders at all levels.
Required Qualifications
Bachelor's degree in a related area.
Minimum 3 years of related experience and 1 year of supervisory or managerial experience.
Certification as a Clinical Trial Professional within one year of appointment.
Experience in project or program coordination, preferably in clinical trials at UCSF or another academic institution.
Knowledge of clinical research, trial recruitment, eligibility, protocol adherence, quality data submission, adverse event reporting, IRB and FDA regulations.
Strong organizational, communication, and interpersonal skills with ability to manage multiple priorities in a fast‑paced environment.
Experience working with oncology patients and sensitive populations.
Proficiency with clinical trial management systems and clinical information applications.
Preferred Qualifications
Advanced degree.
One or more years of experience with industry clinical trials as a CRC.
Experience and knowledge of medical care and Phase I–III oncology trials.
Salary Annual salary range: $115,000 – $130,000.
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.
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Overview The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) Supervisor for the Cutaneous Oncology Program. Under the supervision of the Clinical Research Manager (CRM), the CRC Supervisor will manage and facilitate the day‑to‑day operations of a team of three to six CRCs, ensuring training, performance evaluation, data collection, protocol implementation, and compliance with federal, state, and institutional policies.
Responsibilities
Supervise and train a team of 3–6 CRCs, providing mentorship and performance evaluation.
Oversee day‑to‑day operations of assigned clinical trials, ensuring compliance with Good Clinical Practice and regulations.
Assist the CRM with operational, workload, and protocol implementation issues.
Coordinate study activation, maintenance, and submission of data and adverse event reports.
Develop and implement standard operating procedures to improve efficiency and productivity while safeguarding patient care and data integrity.
Collaborate with cross‑functional teams and maintain relationships with stakeholders at all levels.
Required Qualifications
Bachelor's degree in a related area.
Minimum 3 years of related experience and 1 year of supervisory or managerial experience.
Certification as a Clinical Trial Professional within one year of appointment.
Experience in project or program coordination, preferably in clinical trials at UCSF or another academic institution.
Knowledge of clinical research, trial recruitment, eligibility, protocol adherence, quality data submission, adverse event reporting, IRB and FDA regulations.
Strong organizational, communication, and interpersonal skills with ability to manage multiple priorities in a fast‑paced environment.
Experience working with oncology patients and sensitive populations.
Proficiency with clinical trial management systems and clinical information applications.
Preferred Qualifications
Advanced degree.
One or more years of experience with industry clinical trials as a CRC.
Experience and knowledge of medical care and Phase I–III oncology trials.
Salary Annual salary range: $115,000 – $130,000.
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.
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