Oncology CRA — Global Trials, Travel‑Ready

Worldwide Clinical Trials; United States; Remote; USD 70,000 - 100,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global team in the United States. You will be responsible for site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance and patient safety across multiple therapeutic areas.

You will mentor junior CRAs, review source documents, and manage CRF data with both paper and electronic systems. Willingness to travel is required, and TMF submissions are supported internally.

Qualifications

• 2+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Experience in Oncology and Hematology is required
• Willingness to travel required

Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
• Ensure site compliance with IP receipt, accountability and return or destruction.

Skills

Communication

Organization

Independence

CTMS/EDC

Education

Bachelor’s degree or RN/BSN

Tools

MS Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global team in the United States. You will be responsible for site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance and patient safety across multiple therapeutic areas.

You will mentor junior CRAs, review source documents, and manage CRF data with both paper and electronic systems. Willingness to travel is required, and TMF submissions are supported internally.