ARTO is partnered with a global biopharmaceutical company focused on developing innovative therapies for rare diseases.They’re now looking to appoint an Associate Director, Data Management Science to take ownership of study-related data management activities and drive operational excellence across clinical development programs. This role offers the opportunity to lead on data strategy, process improvement, and ensure high-quality, regulatory-compliant data delivery across global studies.Key reasonability's Lead all study-related data management activities, including protocol review, eCRF design, and development of Data Management and Validation Plans.Collaborate with cross-functional teams to ensure complete, correct, and fit-for-purpose study datasets for statistical analysis.Oversee medical coding, SAE reconciliation, and database lock activities.Manage and guide team members or consultants as needed to achieve departmental goals.Support process improvement and innovation initiatives within data management science.Represent the function in cross-functional study meetings, ensuring alignment and communication between stakeholders.QualificationsAdvanced degree in Data Science, Life Sciences, Statistics, or a related field (PhD/MSc preferred).5+ years’ experience in data management or clinical development within pharma, biotech, or CRO settings.Strong understanding of data standards (CDISC, CDASH) and regulatory compliance (FDA, ICH, GCP).Hands-on experience with data validation, database builds, and clinical programming collaboration.Excellent leadership, communication, and cross-functional coordination skills.