Senior Clinical Research Associate – Oncology, Hematology

This is a fully remote position, open to applicants in France.

📋 Description

• Perform site qualification, initiation, interim monitoring, site management, and study close-out visits.

• Offer mentoring and support to less experienced CRAs and site personnel as necessary.

• Record findings from site visits through detailed written reports.

• Evaluate, oversee, and train study site personnel on adherence to protocols.

• Review safety information of study subjects and ensure informed consent is obtained.

• Execute source document verification to ensure compliance, patient safety, and data integrity.

• Analyze CRFs utilizing paper or electronic data capture systems and assist sites with resolving data queries.

• Provide updates on site-related documentation for inclusion in the Trial Master File (TMF).

• Guarantee site compliance regarding the receipt, accountability, and return or destruction of investigational products.

• Conduct accompanied site visits for the assessment or training of other CRAs.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in both French and English.

• Strong organizational skills with a keen eye for detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, CTMS, and EDC Systems.

• Over 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or RN/BSN in Nursing.

• Willingness to travel is essential.

🏝️ Benefits

• A diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible leadership.

• Opportunities for professional growth and development.

• Mentoring and guidance from seasoned leaders and CRAs.