Early Development Global Study Data Leader

Location: Gent, Belgium Work arrangement: hybrid, minimum 3 days/week in the office About The Job Global Study Data Leader is responsible for leading the end-to-end data management activities and associated quality deliverables for clinical trials including study set-up, conduct, and close‑out, complying with GCP and applicable regulatory guidance. Provide comprehensive data management expertise and support to team members. Coordinate cross‑functional teams globally to ensure the flawless conduct of a clinical trial. Ensure activities are completed according to agreed standards and timelines and serve as the Data Management representative in the study team. About Sanofi We’re an R&D‑driven, AI‑powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities Contributes to the implementation of department initiatives and objectives as well as cross‑functional working groups. Implements and oversees processes and coordinates activities in conjunction with the internal team and Clinical Data Delivery Leader and continually evaluates processes and applications for improvements. Oversee vendor activities to identify risks and ensure that activities are completed according to the SOW, regulations, and with expected quality. Implement quality control strategies and remediations as necessary. Ensure that all external data loading and integration activities (incl. eCOA, IRT, central labs) are well established and that data is loaded as per study timelines (including transfer specifications and reconciliations). Ensure data quality by conducting and/or overseeing data management activities including validation, data review, and safety data reconciliation. Ensure efficient implementation and follow‑up of DM activities for outsourced trials. Develop and drive the retro‑planning for important deliverables such as Interim Analysis, DMC, partial, and final database locks. Ensure clear and prompt updates and escalations to study teams and management. Ensure Database lock readiness by leading the team through the DM lock recommendations and rationale, including implementation of Data Point Lock Strategy. Drive inspection readiness by ensuring ongoing TMF completion for all DM related documents (including documents coming from third parties if applicable). Education Bachelor’s degree or above, preferably in a life science or health‑related field or/and 8‑10 years of Clinical Data Management in the pharmaceutical industry or equivalent can substitute a formal degree. Experience 5+ years of experience in Clinical Data Management in the pharmaceutical industry (or equivalent) is required. 2+ years of project management experience in Data Management is required. Clinical Data Management System experience (CDMS) and understanding of database/programming concepts. Understanding of industry standards, terminologies (e.g., CDISC SDTM, MedDRA, etc.), current regulatory guidelines, and GCP practices regarding Data Management. Vendor management. Solid knowledge of the clinical trial development process. Understanding of risk‑based methodologies and regulations. Experience using Data Visualization tools, e.g. Spotfire, J‑Review, Cluepoints preferred. Core Knowledge, Competencies & Skills Intermediate: Strong Data Management expertise i.e., understanding of Data Management scope and objectives. Solid knowledge of the clinical trial development process and understanding of relevant and current regulatory guidelines, Good Clinical Practice (GCP), industry standards, and practices regarding Data Management. Solid Clinical Data Management System experience (CDMS & EDC) and understanding of database development/programming concepts. Strong collaboration and interpersonal behaviours; manage activities effectively with study team and other DM functions. Establish rapport and collaborate inside and outside the company. Demonstrate flexibility through effective negotiations. Strong communication skills; ensure clear, concise, consistent, and timely communication including risks identification, and escalation. Advanced: Project management skills. Learn and adapt quickly when facing new challenges; ability to think critically and use objective, pragmatic methods to solve multidimensional problems with effective and timely solutions. Mentor and coach new Data Managers on all operational aspects needed for the successful completion of a trial. Expert: Strong experience in data management outsourcing and vendor management, participate and provide Data Management input at BID defense meetings as needed. Be able to present data management topics at CSO level or at a relevant conference. Act as mentor for Data Management supports; responsible for the data quality delivered by team members at the study level. Leadership in driving cultural and structural shifts, shaping company standards in change management excellence. Why choose us? Make your work count by supporting a company that brings life‑changing treatments to millions — and is committed to doing right by patients, communities, and the planet. Drive progress from within by helping simplify, scale, and modernize how a global biopharma business delivers smarter, faster, and more sustainably. Support teams across science, medicine, and operations by building better systems, shaping bold strategies, and enabling innovation at speed. Make an impact across borders and functions, collaborating with leaders to turn complex challenges into real‑world solutions. Advance your career through stretch roles, cross‑functional moves, and development opportunities designed to match your ambition. Thrive in inclusive, high‑performing teams where every role matters and every voice helps shape what’s next. A dynamic and multidisciplinary work environment where your professional background and experience will be highly valued. An exciting career opportunity in an innovative company focused on the treatment options of the future. #J-18808-Ljbffr