Are you a trilingual Senior CRA and want to be part of a growing, dynamic, global company with a very nice familial team spirit? 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. Your focus will be on subjects' rights, safety and well-being and quality of data compliance.Conducting and reporting all types of onsite monitoring visitsDriving the study startup phase (if applicable)Acting as a point of contact for in-house support services and vendorsSupporting quality control, such as compliance monitoring and reports reviewSupporting the regulatory team in preparing documents for study submissions and regulatory approvalBSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experienceIndependent on-site monitoring experience in Belgium, ideally on multiple projects at a timeDemonstrable experience in all types of monitoring visits in Phase II and/or IIIFluency in Dutch, French and EnglishExperience supporting Oncology studies is beneficial, but not essentialAbility to plan, multitask and work in a dynamic team environmentAs you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel.Contract information:~ Freelancer~ September start date~6 FTE (As of Nov/Dec possibility to increase to FT FTE)~ Fully remote