Freelance Senior Clinical Research Associate

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is a freelance (contractor) position in Belgium. Your main responsibilities will include: Conducting and reporting all types of onsite monitoring visits Performing CRF reviews, source document verification and query resolution Be responsible for site communication and management Supervising study activities, timelines, and schedules for each site Acting as a point of contact for in-house support services and vendors Supporting quality control, such as compliance monitoring and reports review BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience Independent on-site monitoring experience in Belgium, ideally on multiple projects at a time Demonstrable experience in all types of monitoring visits in Phase II and/or III Experience supporting Oncology/ Hematology and Infectious disease studies Fluency in Dutch and English, with professional proficiency in French Full and clean driver's license, and the ability to travel Intermediate to Advanced knowledge of MS Office Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.