Oncology Clinical Research Associate – Travel-Ready

Worldwide Clinical Trials; United States; Remote; USD 70,000 - 110,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to monitor sites across multiple therapeutic areas with a focus on Oncology. The role involves qualification, initiation, monitoring visits, and close-out, plus mentoring junior CRAs and ensuring protocol adherence.

Travel is required to sites and TMF documentation is essential. Candidates should have 2+ years as a CRA and a 4-year degree or RN/BSN, with strong English communication and proficiency in Microsoft Office,

Qualifications

• 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.

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.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Skills

Interpersonal skills

Organizational skills

Independent work

English communication

Education

4-year university degree or RN/BSN in Nursing

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to monitor sites across multiple therapeutic areas with a focus on Oncology. The role involves qualification, initiation, monitoring visits, and close-out, plus mentoring junior CRAs and ensuring protocol adherence.

Travel is required to sites and TMF documentation is essential. Candidates should have 2+ years as a CRA and a 4-year degree or RN/BSN, with strong English communication and proficiency in Microsoft Office,