Novartis
### Summary #LI Hybrid (3 days per week on site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Manager We are looking for an experienced and proactive Regulatory Affairs Manager to join our…
### Summary #LI Hybrid (3 days per week on site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Director Novartis is seeking a Global Program Regulatory Director (GPRD) to lead global regulatory strategies…
Job Description Summary #LI Hybrid (3 days per week on site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Manager We are looking for an experienced and proactive Regulatory Affairs Manager to join…
### Summary Job Description Summary As a member of the Knowledge & Content Management Platform team, the Knowledge Management Capability Lead contributes to the strategic vision of Regulatory Affairs and supports the digitalization and centralization of Knowledge Management in Regulatory…
### Summary Our 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…
### Summary Clinical Document Governance Management (CDGM) is accountable for strategy and delivery of clinical document management (CDM) systems, processes, standards and operations of CDM services (including Trial Master File management (TMF), clinical submission readiness, record retention and archiving, Good…
### Summary The Global Program Clinical Head (GPCH) is the global clinical leader responsible for one or more clinical programs across indications, involving one or multiple compounds. The GPCH owns the risk benefit assessment for the program(s), and as the…
### Summary Location: London Office with Hybrid working (12 days per month in the office) #LI Hybrid This role is based in London, UK. Novartis is unable to offer relocation or any visa support for this role: please only apply…
### Summary #LI Hybrid As a Cardiovascular and Metabolism (CVM) Biomarker Lead (BML) (Associate Director) you will lead the CVM disease area biomarker matrix team and be responsible for the development and implementation of “fit for purpose” biomarker strategies and…
Job Description Summary #LI HybridAs a Cardiovascular and Metabolism (CVM) Biomarker Lead (BML) (Associate Director) you will lead the CVM disease area biomarker matrix team and be responsible for the development and implementation of fit for purpose biomarker strategies and…
### Summary When we put our heads together, we can do brilliant work. And when we do brilliant work, we can achieve remarkable things for patients as we positively transform healthcare. We are looking for Senior Administrative Assistants to join…
### Summary #LI Hybrid Novartis has a long term commitment to Global Health including communicable diseases like malaria and non communicable diseases. Novartis first supported sickle cell disease (SCD) care over 50 years ago with the development of chelators for…
### Summary To write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide authoritative documentation related consultancy to other line functions. To coach/mentor and/or train…
### Summary #LI Hybrid As a Clinical Trial Leader, you will be accountable for all aspects of managing and executing early phase clinical trials to deliver high quality data for strategic decision making and drug registration. You will oversee the…
### Summary Accountable for the strategic and operational direction of our Neuroscience Brand Strategy and leading the enterprise wide teams to deliver sales and market share growth with full profit & loss accountability. Role will lead existing brand indication and…
Job Description Summary This is a secondary care sales role responsible for achieving sales targets by promoting and selling the Novartis Breast Cancer product across Greater Manchester and Lancashire. We are open to different levels of experience and the role…
### Summary The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the scientific and medical oversight of assigned clinical trial(s), medical, safety and data monitoring, and reporting of quality data. May be responsible for the scientific and medical…
### Summary Within the Quantitative Sciences drug development function, the Advanced Methodology and Data Science pillar plays a crucial role in enhancing analytical capabilities to support drug development and regulatory decision making. This Associate Director position focuses on optimizing approaches…
Job Description Summary Within the Quantitative Sciences drug development function, the Advanced Methodology and Data Science pillar plays a crucial role in enhancing analytical capabilities to support drug development and regulatory decision making. This Associate Director position focuses on optimizing…
Job Description Summary The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls. Successful candidates will be offered a training position consisting of two rotational assignments, each…
### Summary Locations: London United Kingdom & Barcelona, Spain #LI Hybrid Join Our Vision: At Novartis, we are on a transformative journey in cell and gene therapy, pushing the boundaries of medical innovation building on our heritage pioneering this field.…
### Summary The UK Therapy Area Medical Director for Neuroscience is responsible for driving integrated medical affairs plans for pipeline, launch and marketed products in the neuroscience therapy area and developing and leading the medical TA team. ### About the…
### Summary Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects. Participate in the full lifecycle of producing key data and/or reports in support of data review reporting…
### Summary #LI Remote (possibility to work either remotely or in a hybrid work arrangement) Location: United Kingdom or Ireland Kickstart your career in biostatistics with a distinctive 15 month PhD Graduate Rotation Program, paving the way for a permanent…
### Summary The Clinical Development Director (CDD) is the clinical/scientific and clinical development expert and provides leadership and support to clinical development deliverables and activities within a defined global clinical development program and/or global clinical trial (e.g. clinical development plan,…
### Summary The Medical Manager is accountable for the design and execution of Medical Affairs plans for Solid Tumours (Breast Cancer), providing scientific information, contributing to clinical strategy, collaborating to develop impactful medical education plans, evidence generation plans and implementation…
### Summary The Clinical Development Medical Director (CDMD) is the Global clinical leader of defined and assigned program level activities and deliverables (e.g. submission activities, briefing books etc.), or clinical trial(s), under the leadership of the GPCH or Sr CDMD.…
### Summary As an Immunology Therapeutic Area Biomarker Lead (TABL) in the Biomarker Development (BMD) group, you are accountable for defining and delivering biomarker strategies for an immunology portfolio pillar across multiple drug development programs in early and late phase…
### Summary Responsible for management and coordination of global GVP/GCP inspection & audit participation, conduct of global PS&PV self assessments and contribute to review of draft, new and changed pharmacovigilance/device vigilance regulatory requirements ### About the Role Major accountabilities: Responsible…
Job Description Summary The Study Start Up Senior Lead independently leads the planning and execution of global SSU activities for multiple medium to complex global studies of high priority to ensure timely trial document and task completion to enable country…
Job Description Summary The Senior Study Lead will oversee budget and people allocation within assigned study/studies. Promotes operational excellence through process improvement and knowledge sharing across studies. Fosters an empowered, psychologically safe organization that can navigate a matrix environment, learns,…
Job Description Summary Director, HEOR International co creates and implements strategies to maximize product value, optimize patient access, and outcomes. In this role you will ensure evidence requirements are integrated into clinical plans and product strategies, collaborating with cross functional…
Job Description Summary Responsible independently for the execution and delivery of the GCO supported Radioligand Therapy (RLT) clinical studies of medium to highly complexity and of high priority for novartis, per the Operational Execution Plan (OEP) and clinical study protocol.…
Job Description Summary Novartis is looking for a driven key account manager with a passion for selling to lead one of their top strategic brands of the company in the successful Haematology business unit. You will play an important part…
Job Description Summary We are in search of a Associate Director Biostatistics, with statistical expertise in HTA and Pricing and Reimbursement activities. This role offers the chance to provide statistical solutions to HTA problems. The successful candidate will work closely…