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Senior Clinical Research Associate – Oncology
Worldwide Clinical Trials. Manage clinical research activities at investigative sites participating in Worldwide clinical 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 Development
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 ProcessesData CollectionSafety ReportingStudy Start-Up ActivitiesSite Performance MonitoringInformed Consent ProceduresFull-Service MonitoringRegulatory DocumentationContract and Budget ProcessesStudy Closeout Activities
Soft Skills
CollaborationCommunicationProblem-SolvingAttention to DetailAdaptability
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesPSSVsSIVsIMVsCOVsParticipant SafetyData QualityStudy SuccessTravel 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 activities 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
- Requires travel within the specified region; 8–10 DOS monthly, with some visits remote
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Candidates must reside within the territory
- Ability to travel to investigative sites approximately 8–10 days per month
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Equal employment opportunities