Publication date 2 January 2026 Department Quality, Regulatory and Clinical Affairs Country Belgium Location Mechelen Work arrangement Hybrid Travel percentage 30% Function type Full-time Contract type Employee Experience required Experience working in a similar role in a biotech, diagnostic or pharma company is required. Proven experience in leading scientific projects and presenting scientific results and publications in collaboration with investigators. Proven experience in developing relationships with internal & external scientific stakeholders. Education

Master degree or higher in a scientific orientation, preferably Oncology or equivalent by experience and/or training. PhD is an asset.