Senior Clinical Research Associate - Global Trials Leader

Worldwide Clinical Trials; France; On-site; EUR 55,000 - 75,000; Full time

Job summary

Worldwide Clinical Trials in France is seeking an experienced Clinical Research Associate to ensure the quality of our clinical research programs across sites, from qualification to close-out.

You will mentor junior CRAs, conduct site visits, verify data, review safety information and informed consent, and ensure protocol adherence while traveling as required.

Join a collaborative team that values scientific rigor, patient safety and cross-functional teamwork.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Willingness to travel.

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.

Job description

Worldwide Clinical Trials in France is seeking an experienced Clinical Research Associate to ensure the quality of our clinical research programs across sites, from qualification to close-out.

You will mentor junior CRAs, conduct site visits, verify data, review safety information and informed consent, and ensure protocol adherence while traveling as required.

Join a collaborative team that values scientific rigor, patient safety and cross-functional teamwork.