Clinical Research Supervisor/Protocol Project Manager – Radiation Oncology

Clinical Research Supervisor/Protocol Project Manager – Radiation Oncology

Join to apply for the Clinical Research Supervisor/Protocol Project Manager – Radiation Oncology role at University of California, San Francisco .

Helen Diller Family Comprehensive Cancer Center (HDFCCC)

Full Time

85511BR

Job Summary

We are looking to hire a Clinical Research Supervisor/Protocol Project Manager to help develop, shape, and grow the clinical research team. The UCSF HDFCCC is a fast-paced environment, and the successful candidate will be an independent, detail-oriented individual with drive and focus.

The candidate will manage and facilitate the day-to-day operations of their direct reports (~2-3 clinical research coordinators). Responsibilities include training and evaluating CRC performance, overseeing data collection and reporting, and implementing protocols in compliance with federal, state, and institutional policies.

The supervisor will resolve operational issues, manage workload and protocol implementation, and develop standard operating procedures. The role requires mentoring CRCs to coordinate studies per Good Clinical Practice, aiming for efficiency and productivity without compromising patient care and data integrity.

Success depends on managing performance, maintaining morale, ensuring consistency across disease programs, and providing high-quality customer service. The supervisor will identify training needs and oversee ongoing staff development.

• Note: This is a hybrid role with on-site and remote work; remote days to be determined.

The salary range is $110,000 - $130,900 annually, with final placement based on experience and internal equity. Additional benefits information is available at UC Benefits .

Department Description

The UCSF Helen Diller Family Comprehensive Cancer Center is one of two NCI-designated comprehensive cancer centers in the Bay Area, focusing on laboratory research, clinical translation, patient care, and population health, guided by precision medicine principles.

Required Qualifications

• Bachelor's degree in a related field
• Clinical Trial Professional certification within one year
• At least 3 years’ experience as a CRC in industry clinical trials
• Minimum 1 year of supervisory or managerial experience
• Experience in training research staff and project coordination
• Knowledge of clinical research protocols, IRB, FDA regulations, and oncology terminology
• Experience with clinical trial management systems and data reporting
• Strong communication, organizational, and interpersonal skills

Preferred Qualifications

• Advanced degree
• Experience with oncology trials, UCSF research environment, and systems like OnCore and EPIC

License/Certification

• Clinical Trial Professional certification within one year

About UCSF

UCSF is a leading health sciences university committed to research, education, and patient care, with a diverse community dedicated to equity and excellence.

Pride Values

UCSF values professionalism, respect, integrity, diversity, and excellence, and seeks candidates who contribute to these principles.

Equal Employment Opportunity

UCSF is an equal opportunity employer, considering all qualified applicants without regard to protected characteristics.

Additional Details

Location: San Francisco, CA; Work Style: Flexible; Schedule: Days, Monday-Friday, 8 hours/day.