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About the Role:
The Principal Clinical Data Science Lead will be responsible for managing data management teams, studies, and programs of studies under the general direction of the Senior Manager/Director of Data Management. This role is part of the Early Phase Data Management department and plays a crucial role in ensuring that data collected during trials is managed according to corporate standards and meets regulatory guidelines for data integrity.
The successful candidate will manage a number of fast-moving early phase studies or programs of studies to ensure project objectives are met within budget, to agreed timelines, and to a high level of quality. As a Principal CDSL, you will manage a global team of clinical data management resources, providing input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study-related documents.
Additional responsibilities include reviewing the project contract to ensure that any out-of-scope work is managed promptly and efficiently, managing the overall project budget throughout the life cycle of the project, taking overall responsibility for cost control, timelines, and project quality, negotiating with clients and/or external customers/departments in relation to timelines and key deliverables, and travel (approximately 15%) domestic and/or international.