Impactful Outcomes Research: Clinical Research Assistant I

City of Hope; Duarte (CA); On-site; USD 52,000 - 65,000; Full time

Job summary

City of Hope Beckman Research Institute is seeking a Clinical Research Assistant I to support day-to-day operations of multiple protocols within the Department of Outcomes Research. You will assist with participant prescreening, enrollment, consent support, and data collection, ensuring regulatory compliance and audit readiness.

You will coordinate visits, collect and manage data, and communicate with investigators and regulatory staff.

Qualifications

• Associate’s Degree required; Bachelor’s Degree preferred; experience may substitute education.
• Reading, writing and comprehending medical terminology.
• Reading, identifying and extracting pertinent data from medical records.
• Experience with REDCap is preferred but not required.

Responsibilities

• Manage multiple clinical research protocols with accurate documentation and regulatory compliance.
• Coordinate study activities: scheduling, visit tracking, reminders, questionnaires, specimen workflows, device management, protocol docs.
• Recruit, screen, enroll, consent and follow up with study participants per protocol and guidelines.
• Collect, manage and submit study data with data integrity and protocol adherence.
• Perform protocol-specific duties including specimen collection, processing and safety.
• Monitor activities for deviations and communicate findings to investigators and leadership.
• Train and mentor new staff and foster collaboration among participants and healthcare teams.
• Work independently, support special projects and pursue ongoing professional development.

Skills

Medical terminology

Data extraction

Data entry

Clinical research

Education

Associate’s Degree

Bachelor’s Degree preferred

Tools

REDCap

Job description

City of Hope Beckman Research Institute is seeking a Clinical Research Assistant I to support day-to-day operations of multiple protocols within the Department of Outcomes Research. You will assist with participant prescreening, enrollment, consent support, and data collection, ensuring regulatory compliance and audit readiness.

You will coordinate visits, collect and manage data, and communicate with investigators and regulatory staff.