Clinical Research Associate – Oncology
Location: Los Angeles, California / San Diego, California (Remote-Based with Regional Travel)
Job ID: JR141761
Employment Type: Full-Time
Work Model: Remote (Up to 50% Travel Required)
Role Overview
An established global pharmaceutical/CRO organization is seeking a Clinical Research Associate (CRA) – Oncology to support oncology clinical trials across the Southeast region of the United States. This remote-based role is ideal for an experienced oncology CRA residing in Los Angeles, CA, with convenient access to major hub airports to support regional travel.
The CRA will serve as the primary liaison between investigational sites and the sponsor, ensuring regulatory compliance, patient safety, and high-quality data delivery throughout all phases of the clinical trial lifecycle.
Key Responsibilities
Act as the primary point of contact between investigational sites and sponsor teams
Conduct all types of monitoring visits including site selection, site initiation, routine monitoring, and close-out visits
Ensure site compliance with ICH-GCP guidelines, sponsor SOPs, and local regulatory requirements
Maintain accurate and up-to-date records in CTMS and eTMF systems
Monitor patient safety, ensuring accurate and timely reporting of AEs, SAEs, and PQCs
Support and track investigator site training and compliance documentation
Oversee investigational product accountability, storage, return, and destruction processes
Review source documentation, resolve data queries, and ensure high-quality, timely data entry
Support subject recruitment and retention strategies at the site level
Document site performance and proactively escalate risks, protocol deviations, or compliance issues
Collaborate cross-functionally with Clinical Trial Assistants (CTAs), Local Trial Managers (LTMs), and Clinical Trial Managers (CTMs)
Assist with site budget tracking and payment follow-up where applicable
Required Qualifications
Bachelor’s degree in Life Sciences or related field, or qualified Registered Nurse (RN)
Eligibility to work in the United States without visa sponsorship
Minimum 2+ years of on-site clinical monitoring experience in a pharmaceutical company or CRO
Direct experience monitoring oncology clinical trials (mandatory)
Strong knowledge of ICH-GCP and U.S. regulatory requirements
Experience using clinical systems such as CTMS and eTMF
Excellent communication, problem-solving, and organizational skills
Willingness and ability to travel up to 50% for on-site monitoring visits
Preferred Profile
Based in or near Los Angeles, CA, with access to major hub airports
Proven ability to manage multiple sites and competing priorities in oncology studies
Strong documentation and audit-readiness experience
Why Consider This Opportunity
This role offers the opportunity to contribute to cutting-edge oncology research while working remotely within a structured and collaborative clinical operations environment. As a Clinical Research Associate specializing in oncology, you will directly impact patient safety, regulatory compliance, and the successful execution of complex cancer trials.
SEO & GEO Keywords: Clinical Research Associate Oncology Jobs USA, CRA Jobs Los Angeles CA, Oncology Clinical Trials Monitoring Jobs, Remote CRA California, Oncology Monitoring Experience Required, ICH-GCP Clinical Research Careers, Pharmaceutical CRA Jobs United States
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