Tasks & Responsibilities:

• Entertain daily contacts with a team of CRAs active on the project
• Assume project management responsibilities for assigned clinical studies; participate in project planning, budgeting and expense analysi
• Contribute to the clinical protocol study design, development of CRFs, quality assurance, data management and reporting activities
• Identify and evaluate issues related to the project and implement resolutions
• Assume in-house monitoring, assign field monitors to projects as needed and required by GCP; perform on-site monitoring as needed by GCP
• Participate in Investigator selection, recruitment and training and provide final recommendations
• Plan and create presentations of clinical research study information

• Bachelor in Nursing or University degree (Biomed, Sciences, Physical Education, Physiotherapy, Biology), or equivalent through experience
• Able to work under pressure and to meet deadlines in a highly regulated and procedural environment
• Excellent language skills (English, Dutch, French)
• Strong organizational and excellent communication skills
• Able to multi-task and prioritize
• Result-driven team player
• Have a mature, responsible and flexible attitude
• Quality oriented with commercial awareness
• Have excellent people-skills
• Knowledge of ICH GCP and European Directives is a must
• Experience as CPM is a must
• Willingness to travel