Oncology Clinical Research Coordinator - 259140

Oncology Clinical Research Coordinator (Los Angeles, CA)Format: Direct Hire

Location: Los Angeles, CA (90067)Hours: Full time, Monday - Friday, 8am-5/6pmPay: $72,000 - $90,000

Responsibilities

Coordinate and conduct protocol-required study visits and procedures for oncology clinical trials, with preference for experience supporting Phase I studies.Obtain and document informed consent in accordance with federal regulations, GCP, and IRB requirements.Accurately document patient assessments, observations, test results, and other study-related activities in source documents and CRFs/eCRFs.Schedule and manage participant visits while ensuring adherence to protocol timelines and sponsor requirements.Recruit and screen eligible participants to meet study enrollment goals while maintaining ethical and regulatory compliance.Monitor and report adverse events (AEs) and serious adverse events (SAEs) in accordance with sponsor and regulatory timelines.Maintain accurate records and accountability for study materials, investigational products, and lab supplies.Ensure compliance with GCP, ICH guidelines, HIPAA regulations, and site SOPs.Communicate regularly with investigators, study team members, sponsors, and other stakeholders to ensure smooth study operations.Participate in investigator meetings, trainings, and continuing education to remain current on clinical research regulations and best practices.Represent the organization professionally when interacting with patients, sponsors, IRBs, and clinical partners.Perform additional study-related duties as assigned.

Qualifications

Bachelor’s degree preferred but not required.2+ years of experience as a Clinical Research Coordinator, with oncology experience strongly preferred.Phase I oncology clinical trial experience preferred.Strong knowledge of clinical research regulations, GCP, and protocol compliance.Preferred Skills:Strong organizational and multitasking abilities in a fast-paced research environment.Excellent written and verbal communication skills.Proficiency with Microsoft Office / Office365 and clinical research documentation systems.Ability to collaborate effectively with cross-functional teams and manage competing priorities.Strong attention to detail, problem-solving, and process improvement skills.