Senior Clinical Research Associate – Oncology

Worldwide Clinical Trials

. Manage research activities at sites participating in Worldwide’s clinical research projects .

Posted 9/28/2026full-timeRemote • North Carolina • 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, ensuring compliance with regulatory requirements, and effectively training site personnel. Proficient in utilizing Microsoft Office, CTMS, and EDC Systems to support clinical trials, with a strong focus on Oncology and CAR-T methodologies.

Highest-signal resume keywords

Clinical Research Associate ExperienceOncology ExpertiseCAR-T ExperienceMicrosoft Office ProficiencyCTMS and EDC Systems Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ManagementRegulatory Document CollectionData Collection TrainingSafety-Event ReportingStudy Start-Up ActivitiesSite Maintenance ManagementStudy Initiation VisitsInformed-Consent ComplianceRemote Site Management

Soft Skills

Interpersonal CommunicationOrganizational SkillsAttention to DetailAbility to Work Independently

Tools & Technologies

Microsoft OfficeCTMSEDC Systems

Industry Keywords

Clinical ResearchOncologyCAR-TRegulatory ComplianceSafety-Event Reporting

About the role

Key responsibilities & impact

Manage research activities at sites participating in Worldwide’s clinical research projects
Identify potential sites to participate in clinical research
Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations
Train sites to collect data properly and report potential safety-related events
Manage site activities during study maintenance
Close down research activities at sites once studies conclude
Conduct study initiation visits (SIVs)
Ensure compliance with informed-consent procedures, safety-event reporting, and applicable regulatory requirements
Perform most site-management efforts remotely

Requirements

What you’ll need

Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Current experience in Oncology is required
CAR-T experience is desired
Fluent in written and verbal English required
Candidates must reside in the contiguous United States
Willingness to travel regionally required

Benefits

Comp & perks

Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
Regular touchpoints and coaching conversations with Line Manager
Clear career path and professional development that can lead to Clinical Trial Manager roles
Accessible Executive Leadership team
Competitive benefits package depending on location