Oncology Clinical Research Coordinator

University of California - San Francisco; San Francisco (CA); On-site; USD 70,000 - 98,000; Full time

Job summary

University of California - San Francisco is seeking a Clinical Research Coordinator to manage and coordinate research protocols under the supervision of the PI and Clinical Research Manager. You will oversee data collection, regulatory compliance, and overall study operations across multiple concurrent trials.

The role includes coordinating participant recruitment, scheduling visits, data entry into OnCore and EMR systems, maintaining regulatory documents, and supporting audits.

Qualifications

• Experience in clinical research or related training in a clinical setting.
• Familiarity with specimen processing and data collection procedures.
• Proficiency with OnCore or similar clinical trial management systems.
• Attention to detail and strong written and verbal communication skills.
• Ability to multi-task in a fast-paced research environment.

Responsibilities

• Identify subjects, screen and enroll study participants and coordinate recruitment strategies.
• Schedule study visits, administer questionnaires, collect medical history and perform procedures.
• Maintain data integrity and ensure accurate data entry into study databases.
• Prepare regulatory documents, maintain study records, and ensure compliance with regulatory guidelines.
• Communicate with PI, supervisor and staff; assist with audits and quality improvements.

Skills

Clinical research coordination

Regulatory compliance

Data management

OnCore

IRB/Regulatory knowledge

Patient recruitment

Education

High School diploma or equivalent

Experience in clinical research

Tools

OnCore

Excel

Electronic Medical Records

Job description

University of California - San Francisco is seeking a Clinical Research Coordinator to manage and coordinate research protocols under the supervision of the PI and Clinical Research Manager. You will oversee data collection, regulatory compliance, and overall study operations across multiple concurrent trials.

The role includes coordinating participant recruitment, scheduling visits, data entry into OnCore and EMR systems, maintaining regulatory documents, and supporting audits.