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.

• Provide mentorship and support to junior CRAs and site personnel as necessary.

• Document findings from site visits through written reports.

• Evaluate, monitor, and provide training to study site staff on adherence to protocols.

• Review safety information regarding study subjects and informed consent documents.

• Conduct source document verification to ensure compliance, patient safety, and data accuracy.

• Review Case Report Forms (CRFs) utilizing both paper and electronic data capture systems.

• Assist study sites in resolving data queries.

• Update site-related documentation for inclusion in the Trial Master File.

• Ensure site compliance concerning the receipt, accountability, and return or destruction of investigational products.

• Conduct accompanied site visits for the assessment or training of other Clinical Research Associates.

⛳️ Requirements

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

• Outstanding organizational abilities with a keen eye for detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC) systems.

• More than 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree from a four-year university or a Registered Nurse (RN) / Bachelor of Science in Nursing (BSN).

• Willingness to travel is required.

🏝️ Benefits

• Equal employment opportunities regardless of protected characteristics.

• Supportive, diverse, and inclusive work environment.

• Culture focused on collaboration and creativity.

• Opportunities for mentoring and guidance.

• Global team environment.

• Professional growth and development opportunities.