Head, Compliance Clinical Quality AssuranceOur Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic areas and platform depth and capabilities – all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to. Apply today – we will thrive together!About the RoleJob Purpose: Are you ready to become the Head, Compliance Clinical QA? As primary quality contact for Business Process Owners (BPOs) in Development, you are responsible for end-to-end quality oversight of clinical processes, ensuring compliance with Health Authorities requirements and internal standards. The individual will be a deep thinker and data-focused. This will mean extracting information from different data sources, summarizing in a way that is actionable and identifying desired behaviors. You will be synergizing many elements; highest risk, what the data highlights, how many and where audits take place, time constraints, and fixing any risks ahead of time for Novartis in the clinical space.Key Responsibilities:Actively drive a culture of quality and successfully embed a quality mindset across Development by forging strong business partnerships, positively impacting business deliverables, and effectively implementing the strategy, mission, and purpose of RDQ.Guide Quality System Owners (QSOs) and BPOs in the development of a robust strategy for clinical process changes, considering interdependencies and guiding respective risk business owners in all aspects of risk management.Collaborate closely with BPOs to prepare for audits, actively participate, support formulating robust CAPA plans, ensuring comprehensive review and flawless implementation.Collaborate closely with the Head GCP Inspection Management and GCP Inspection Project Manager(s) when a GCP Health Authority Inspection is announced, promptly identifying potential risk areas that may impact the process.Guide BPOs in preparing for specific presentations and deliverables requested during inspections.Proactively address potential gaps and risks while identifying valuable opportunities for continuous improvement. Drive continuous improvement through data-generated insights for the respective clinical processes, fostering a culture of excellence.Your Experience:Master's degree in life sciences / healthcare, M.D, Ph.D or MBA is desired.At least 10 years of involvement in regulated activities (GCP/PH), clinical development, and/or QA position in the pharmaceutical drug development.Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
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