Clinical Research Coord

City of Hope; Duarte (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

City of Hope in Duarte, CA is seeking a Clinical Research Coordinator (CRC) to maintain data integrity across oncology studies, manage case report forms, and support regulatory compliance.

You will work with multiple investigators, coordinate site visits, ensure audit-ready documentation in CTMS, and uphold GCP, FDA, NIH, and HIPAA standards. Minimum education is a Bachelor's degree with 2+ years oncology trial experience.

Qualifications

• Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Experience with oncology clinical trials in an academic setting (2+ years).
• Familiarity with IRB requirements and consent processes.

Responsibilities

• Maintain data integrity across assigned studies and complete case report forms accurately.
• Schedule sponsor monitoring visits and ensure data is audit-ready per contract.
• Manage CTMS records and ensure protocol adherence and regulatory compliance.
• Collaborate with investigators and study teams to resolve data queries and monitor study progress.

Skills

GCP

FDA regulations

NIH guidelines

HIPAA regulations

Education

Bachelor's Degree

Tools

CTMS

Job description

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.

As a successful candidate, you will:

The Clinical Research Coordinator (CRC) will be responsible for maintaining data integrity of multiple assigned research studies for 3 Principal Investigators across various Disease Teams. They are responsible for abstracting data, completing case report forms (CRFs) and answering queries. They schedule and meet with sponsor monitor visits and maintain data in an audit ready state, meeting the requirements of the contract. CRCs are also responsible for ensuring compliance to the research protocol and all appropriate regulations. It is their responsibility to create and maintain the research record and maintenance of patient information in the clinical trials management system (CTMS).

The CRC must be well versed in Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPAA regulations. If not already, s/he must become familiar with institutional policy and procedures regarding conducting multiple clinical research trials. Develop and maintain knowledge of institutional protocol submission procedures and requirements. The CRC must be able manage multiple medium to high complexity research projects ensuring quality research conduct, achievement of expected timelines and deliverables, and efficient use of human and practical resources. The CRC must be able to work as a member of the clinical research team with positive and timely written and verbal communication, including sharing information up, down and laterally. This includes communicating protocol deviations or issues with study execution. They are to ensure protocol adherence by understanding, communicating and making sure the study parameters are ordered and carried out per protocol requirements. The CRC seeks supervision appropriately, prioritizes appropriately, completes work in a timely manner and demonstrates accuracy in all details.

Essential Functions

• Ensure all protocol-required procedures are ordered and completed, prepare and transport or ship biospecimens in accordance with IATA requirements, and support participant safety through timely adverse event reporting.
• Abstract accurate source data, complete paper and electronic case report forms, maintain patient source documentation, obtain external records and images, and resolve data queries within required timelines.
• Maintain assigned studies in an audit-ready state by following Good Clinical Practice, sponsor, institutional, and regulatory documentation and reporting requirements.
• Coordinate and participate in study meetings, monitoring visits, audits, and source data verification; review monitoring findings and resolve outstanding protocol and data issues.

Your qualifications should include:

Minimum Education:Bachelor’s Degree. Experience may substitute for minimum education requirements. (Associate Degree plus minimum of 2 years of experience).
Minimum Experience:Two or more years of experience related to the management and conduct of oncology clinical trials in an academic setting. Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.

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.

To learn more about our Comprehensive Benefits, please CLICK HERE.