Hardeep Banwait

Global Clinical Study Manager @阿斯利康

Cambridge, GB

Oversight to ensure study delivery• Lead preparation of delegated study documents, including external service provider related documents• Maintain and facilitate interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.• Contribute to the planning and conduct of internal and external meetings • Ensure the supply of Investigational Product and study materials by liaising with Clinical Supply Chain or external service providers.• Contribute to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.• Ensure that all study documents are complete and verified for quality in Trial Master File.• Provide support with budget management, including external service provider invoice reconciliation.• Working to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready.• Support with overall project management• Support to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study.• Work on assignments on non-drug project work in process improvements and/or leading improvement projects.

Sheffield Hallam University

BSc. (Hons) Biomedical Science, Biomedical Sciences