Company: Novartis

Job Description Summary Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, [...]Read More... from CFO Northern Cluster/ UK&IE See details

Summary The Financial Controls and Compliance (FCC) Process Expert – PIN (Production and Inventory) and PCA (Product Cost Accounting) is responsible for overseeing and identifying financial E2E process risks and control requirements relevant to the NFCM PIN and PCA framework. This role involves close collaboration with relevant stakeholders to assess risks and provide advice on [...]Read More... from Global FC&C Process Expert (Senior Manager) PIN-PCA See details

Job Description Summary – Understand complex and critical business problems from a variety of stakeholders and business functions, formulate integrated analytical approach to mine data sources, employ statistical methods and machine learning algorithms to contribute solving unmet medical needs, discover actionable insights and automate processes for reducing effort and time for repeated use. Manage the [...]Read More... from Associate Director Data Science See details

Summary Location: London, UK #LI-Hybride As part of the Novartis vision to be a trusted leader in changing the practice of medicine, Novartis is committed to comply with all relevant trade sanctions and export controls in our operations worldwide. This global Senior Legal Counsel position is responsible for providing legal leadership and strategic counsel as [...]Read More... from Senior Legal Counsel, Trade Sanctions See details

Job Description The GCO Budget Manager is responsible for providing each assigned Clinical Trial Team (CTT) accurate actual spend vs. endorsed budget as per Operational Execution Plan (OEP) requirements. He / She may be assigned to a portfolio of trials with low to medium complexity, volume, and priority (in trial set-up, lifetime costs, etc.). He [...]Read More... from GCO Budget Manager See details

Job Description Summary Primary Location: White City, London, UK Working model: Hybrid working model (which requires 12 days per month in the office) Note: Novartis is not able to offer relocation support for this role. Please only apply if this location is accessible for you. About this role: As a key player in our team, [...]Read More... from Senior Patient Safety Specialist See details

Summary Location: London, UK Working model: Hybrid working model (12 days per month in the office) Note: Novartis is unable to provide relocation or visa support for this position. The Senior Development Quality Assurance Specialist assists with quality oversight for activities undertaken in all Novartis entities in a country to assure compliance with relevant Good [...]Read More... from Senior Development Quality Assurance Specialist See details

Summary The Early Development, Associate Director, Statistical Programming, is responsible for all statistical programming aspects of one or more drug development programs or indication programs within the Early Development space. As a program lead, the Associate Director ensures cross-functional collaboration within and outside AQS and decision-making for assigned trials/programs in drug life cycle management. They [...]Read More... from Associate Director, Statistical Programming See details

Job Description Summary This is a sales role responsible for achieving sales targets by promoting and selling the Novartis Breast Cancer product covering the South Wales area. We are open to different levels of experience and the role may be titled Senior KAM depending on experience. Job Description Location: This position will cover the South [...]Read More... from KAM Oncology – South Wales See details

Job Description Summary – Provide highly advanced expert support & functional and technical leadership to ensure the scientific integrity/validity for clinical development, early development, and/or research projects. Develops and applies biostatistics and programming methods to ensure valid conclusions. Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries. [...]Read More... from Associate Director Biostatistics See details