Freelance Senior Clinical Research Associate

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

📋 Description

• Execute and document various onsite monitoring visits.

• Conduct reviews of CRFs, verify source documents, and resolve queries.

• Oversee communication with sites.

• Manage study activities, timelines, and schedules for each site.

• Serve as a liaison for in-house support services and vendors.

• Assist in quality control processes, including compliance monitoring and report evaluations.

• Develop and sustain relationships with clinical sites and investigators.

• Ensure adherence to timelines, targets, and standards for clinical research projects.

• Prioritize the rights, safety, and welfare of subjects, as well as the quality of data compliance.

⛳️ Requirements

• Bachelor’s or Master’s degree in Life Sciences (or a related field), or an equivalent combination of education, training, and experience.

• Independent onsite monitoring experience in Belgium, preferably managing multiple projects simultaneously.

• Proven experience in conducting all types of monitoring visits for Phase II and/or III studies.

• Background in supporting Oncology/Hematology and Infectious Disease studies.

• Proficiency in Dutch and English, with professional working knowledge of French.

• Possession of a full and clean driver's license, and the capability to travel.

• Intermediate to advanced proficiency in MS Office applications.

🏝️ Benefits

• Opportunities for professional development and career advancement.

• Assistance and support throughout the recruitment process.