Freelance Senior Clinical Research Associate

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

📋 Description

• Conduct and document all varieties of onsite monitoring visits

• Execute CRF evaluations, verify source documents, and resolve queries

• Oversee communication with sites

• Manage site operations

• Supervise study activities, timelines, and schedules for each location

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

• Assist with quality control, including compliance monitoring and report reviews

• Establish and nurture relationships with clinical sites and investigators

• Safeguard subjects’ rights, safety, well-being, and ensure data quality compliance

⛳️ Requirements

• BSc or MSc 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 various types of monitoring visits during Phase II and/or III

• Background in supporting Oncology/Hematology and Infectious disease studies

• Proficient in Dutch and English, with professional proficiency in French

• Possess a full and clean driver's license

• Willingness to travel

• Intermediate to advanced proficiency in MS Office

🏝️ Benefits

• Opportunities for professional development and career advancement

• Guidance and support throughout the recruitment process