Senior Clinical Research Associate – Oncology

Worldwide Clinical Trials

. Manage clinical research activities at investigative sites participating in Worldwide clinical studies .

Posted 10/27/2026full-timeRemote • United StatesSenior💰 $97,000 - $193,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research activities, including site management, regulatory compliance, and monitoring of Oncology clinical trials. Proven ability to train site personnel and ensure data quality and participant safety throughout the study lifecycle.

Highest-signal resume keywords

Clinical Research ManagementOncology Clinical Trials MonitoringRegulatory ComplianceSite ManagementTraining and Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesSite Performance MonitoringRegulatory DocumentationContract and Budget ProcessesData CollectionSafety ReportingFull-Service MonitoringInformed Consent ProceduresStudy Closeout ActivitiesHematology Experience

Soft Skills

CollaborationCommunicationProblem-SolvingOrganizational SkillsAttention to Detail

Certifications & Qualifications

Bachelor's DegreeNursing Degree

Industry Keywords

Clinical Research AssociateInvestigative SitesWorldwide Clinical StudiesPSSVsSIVsIMVsCOVsParticipant SafetyWest Coast TerritoryTravel Requirements

About the role

Key responsibilities & impact

Manage clinical research activities at investigative sites participating in Worldwide clinical studies
Identify and assess potential research sites
Coordinate study start-up activities, including regulatory documentation and contract and budget processes
Conduct PSSVs, SIVs, IMVs, and COVs
Train site personnel on protocol requirements, data collection, and safety reporting
Monitor site performance and provide ongoing study maintenance support
Ensure informed consent, safety reporting, and regulatory compliance
Partner with sites and study teams to drive data quality, participant safety, and study success
Support site closeout and completion of study requirements
Travel to investigative sites approximately 8–10 days per month

Requirements

What you’ll need

Bachelor's Degree or a Nursing Degree
5+ years as a regional, traveling Clinical Research Associate
Required experience monitoring Oncology clinical trials
Hematology experience preferred
Ability to travel within the specified region, 8–10 days per month
Experience in full-service monitoring preferred
Strong knowledge of clinical trial processes, site management, and regulatory requirements
Candidates must reside within the West Coast territory of the United States

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Equal employment opportunities