Senior Clinical Research Associate – Oncology, Hematology

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

📋 Description

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

• Offer mentorship and support to less experienced Clinical Research Associates (CRAs) and site personnel as necessary.

• Record findings from site visits through comprehensive written reports.

• Evaluate, monitor, and train study site personnel on adherence to protocols as required.

• Examine study subject safety information and informed consent documents.

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

• Review Case Report Forms (CRFs) utilizing paper or electronic data capture systems, and assist sites in resolving data queries.

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

• Ensure site compliance regarding investigational product (IP) receipt, accountability, and return or destruction.

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

⛳️ Requirements

• Minimum of 2 years of experience as a Clinical Research Associate.

• Bachelor’s degree or RN/BSN in Nursing from a recognized institution.

• Required experience in Oncology and Hematology.

• Willingness to travel as needed.

• Exceptional interpersonal, oral, and written communication skills in English.

• Excellent organizational skills with a strong attention to detail.

• Ability to work independently with minimal supervision.

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

🏝️ Benefits

• Participation in global team events.

• Collaborative and supportive team environment.

• Commitment to a diverse and inclusive workplace.