Senior Clinical Research Associate, Oncology

Worldwide Clinical Trials

Senior Clinical Research Associate responsible for overseeing clinical research activities in Oncology projects. Collaborating with sites and ensuring compliance with regulatory requirements while managing research initiatives.

Posted 5/11/2026full-timeRemote • North Carolina • 🇺🇸 United StatesSeniorWebsite

About the role

Key responsibilities & impact

Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
Conduct study initiation visits (SIVs)
Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

Requirements

What you’ll need

5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in Oncology is required
Proficiency in Microsoft Office, CTMS, and EDC Systems

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical researchstudy initiation visitsinformed consentsafety reportingregulatory complianceOncology

Certifications

4-year university degreeNursing Degree