Senior Clinical Research Associate

Worldwide Clinical Trials

Senior Clinical Research Associate managing clinical research projects involving registries and non-interventional studies at Worldwide. Ensuring compliance and proper training while overseeing site activities.

Posted 4/16/2026full-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
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort
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 RN/BSN in Nursing
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems

Benefits

Comp & perks

health insurance
inclusive environment that encourages collaboration and creativity

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical researchstudy initiation visitsinformed consentregulatory compliance

Soft Skills

interpersonal skillsoral communicationwritten communicationorganizational skillsattention to detailability to work independently

Certifications

RNBSN