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Senior Clinical Research Associate – Oncology
Worldwide Clinical Trials. Manage clinical research activities at investigative sites participating in Worldwide Clinical Trials studies .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research activities, including site management, regulatory compliance, and monitoring 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 Support
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesRegulatory DocumentationContract and Budget ProcessesData CollectionSafety ReportingSite Performance MonitoringStudy Start-Up ActivitiesStudy CloseoutFull-Service MonitoringInformed Consent
Soft Skills
CollaborationCommunicationProblem-SolvingLeadership
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesPSSVsSIVsIMVsCOVsData QualityParticipant SafetyEast Coast TerritoryTravel Requirements
About the role
Key responsibilities & impact- Manage clinical research activities at investigative sites participating in Worldwide Clinical Trials 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 support during study maintenance
- 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
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
- Must reside within the East Coast territory
- Requires travel within the specified region; 8–10 days on site monthly
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Equal employment opportunities