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Senior Clinical Research Associate / Clinical Research Associate II - Oncology -

Parexel•United States•🌍 Remote
Full-time3-7
👁️ 0 views•📝 0 applications•Posted 8/20/2026•Expires 10/19/2026
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Job Description

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is seeking a Senior Clinical Research Associate or Clinical Research Associate II who is experienced in Oncology On-Site Monitoring on the West Coast, US! Job Purpose: The Senior Clinical Research Associate (Sr.

CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr.

CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e. g. enrollment, database release), to safeguard the quality of investigator sites (e. g.

patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Sr.

CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.

Key Accountabilities: Oversight of Monitoring Responsibilities and Study Conduct Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and s

Required Skills

OncologyClinical ResearchClinical TrialsGood Clinical Practice (GCP)Site MonitoringInvestigator Site ManagementProtocol CompliancePatient SafetyClinical Trial RegulationsDatabase ReleaseSite Quality AssuranceEnrollment ManagementSite Close-OutStudy Monitoring Plan (SMP)Regulatory ComplianceWest Coast US ExperienceSite Care Partner (SCP) CollaborationStakeholder Engagement

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