The Clinical Data Acquisition and Strategy Manager defines and facilitates the participant data journey, identifying participant data sources, transport methods, ingestion to client ecosystem and mitigating potential challenges to ensure understanding, consistency and integrity of the participant data. The role will collaborate with technical and clinical teams across Client to define participant data requirements and challenges to provide short- and long-term solutions. Responsibilities include providing technical and procedural guidance on data ingestion and chain of clinical data custody, and identifying participant data sources and document.

As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that advance our understanding of new therapies. You will contribute to the development of innovative treatments by applying scientific expertise and collaborating with multidisciplinary teams throughout the research process.

As a Senior Clinical Scientist, you will provide scientific and clinical support from ongoing early and late-stage clinical trials with an emphasis on protocol-specific, in-life clinical data monitoring activities. This role will also serve as a point of contact for CROs, investigators and study staff in day-to-day safety monitoring. The position requires experience in analysis and interpretation of clinical data.