Senior Clinical Research Associate – Global Trials

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

Job summary

Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to support site qualification, monitoring, and study close-out visits across trials. You will mentor junior CRAs and ensure protocol adherence, safety reporting, and data integrity through on-site or remote reviews.

The role requires 5+ years in CRA, a 4-year degree or RN/BSN, and willingness to travel to sites as needed. Strong English and French communication skills are essential.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• 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.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Skills

Communication (English & French)

Education

Bachelor's degree or RN/BSN

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to support site qualification, monitoring, and study close-out visits across trials. You will mentor junior CRAs and ensure protocol adherence, safety reporting, and data integrity through on-site or remote reviews.

The role requires 5+ years in CRA, a 4-year degree or RN/BSN, and willingness to travel to sites as needed. Strong English and French communication skills are essential.