DPS Clinical Research Assistant I – Outcomes Research

Mobile; Duarte (CA); On-site; USD 47,000 - 53,000; Full time

Job summary

City of Hope's Beckman Research Institute seeks a Clinical Research Assistant I for the Outcomes Research department in Duarte. You will support daily protocol operations, prescreen participants, assist with recruitment and consent, coordinate visits, and ensure data integrity and regulatory readiness.

You will collect and manage study data, aid in specimen workflows where applicable, and communicate findings to investigators and staff while maintaining independence within approved protocols.

Qualifications

• Associate’s degree required; bachelor’s preferred; experience may substitute for education.
• Competence with medical terminology in reading and writing.
• Ability to read and extract pertinent data from medical records.
• REDCap experience is a plus but not required.

Responsibilities

• Support day-to-day operations of multiple clinical research protocols.
• Coordinate participant prescreening, recruitment, consent support, and visits.
• Data entry, quality review, and regulatory file maintenance.
• Audit readiness and regulatory communication with teams and sponsors.
• Maintain protocol adherence and assist with study documentation.

Education

Associate's degree

Bachelor's degree preferred

Medical terminology proficiency

Medical record data extraction

REDCap experience

Job description

DPS Clinical Research Assistant I – Outcomes Research – (10036051)

Description

Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we’re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

A Clinical Research Assistant I is available within the Department of Outcomes Research. You will support the day-to-day operations of multiple clinical research protocols to ensure efficient study conduct, regulatory compliance, accurate documentation, and timely data collection. Your responsibilities will include participant prescreening, recruitment, informed consent support, study visit coordination, data entry and quality review, regulatory file maintenance, audit readiness, and communication with investigators, clinical teams, regulatory staff, sponsors, vendors, and other internal and external collaborators. You must also exercise independent judgment within established protocols, institutional policies, and Good Clinical Practice standards.

As a successful candidate, you will:

• Manage multiple clinical research protocols, ensuring accurate documentation, participant registration, and compliance with study and regulatory requirements.
• Coordinate all study activities, including participant scheduling, visit tracking, reminders, questionnaires, specimen workflows, device management, and protocol-specific documentation.
• Recruit, screen, enroll, consent, and follow up with study participants in accordance with protocol and institutional guidelines.
• Collect, manage, analyze, and submit study data while maintaining data integrity and adherence to protocol requirements.
• Perform protocol-specific clinical and research duties, including specimen collection, processing, handling, and safety compliance.
• Monitor research activities for protocol adherence, identify issues or deviations, and communicate findings to investigators and leadership.
• Train and mentor new clinical research staff while fostering collaborative relationships with participants, investigators, and healthcare teams.
• Function independently with minimal oversight, support special projects, maintain an efficient work environment, and engage in ongoing professional development.

Qualifications

Your qualifications should include:

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

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

• Primary Location: United States-California-Duarte
• Job: Clinical Research Work Force Type: Onsite
• Shift: Days
• Job Posting: Nov 6, 2026
• Minimum Hourly Rate ($): 33.800000
• Maximum Hourly Rate ($): 38.252300