About the job Department – Clinical Reporting Unit Are you an experienced Medical Writing specialist with a strong background in regulatory medical writing? Do you have a passion for clear and concise communication of clinical data? We are looking for…

About the job Summary Lead, support, and report independent GCP/PV audits according to the Novartis Quality Systems and the current GCP/PV regulations to assess compliance with applicable regulations, standards, and guidance documents. Review and approve corrective action plans in support…

About the job Summary Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial…