Novartis
### Summary Responsible for overseeing the product portfolio and project management process in a sub part of the overall organization (major region, region, country, group, division, subsidiary, or other sub part) ### About the Role Major accountabilities: Provides Project Portfolio…
Summary Location: London, United Kingdom #LI Hybrid Internal job title: Senior Expert Data Science / Data & AI Engineer About the Role: Complex data are integral to our work in clinical studies. This position is part of a newly established…
Job Description Summary Leads development of scientific communication platform (scientific statements, lexicon, and scientific narrative) aligned with Therapeutic Areas for launch assets/disease area, including publication and medical education strategy and execution. Job Description Major Accountabilities: Leads the development, implementation, and…
Job Description Summary We deliver professional Global Security (GS) investigations throughout the Europe, Middle East and Africa region, representing the vanguard of Novartis’s Corporate Governance response to internal fraud, corruption and other alleged internal misconduct, including violation of company policies,…
Job Description Summary As our Clinical Development Director in Neurosciences you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. In addition, you may be responsible for the clinical…
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 our…
Summary LOCATION: London, UK or Barcelona, Spain ROLE TYPE: Hybrid working, #LI Hybrid As Associate Director (AD) Scientific Engagement Governance you will be supporting the implementation of an integrated Novartis (NVS) strategy, enterprise processes and standards to ensure adherence and…
Summary Leads development of scientific communication platform (scientific statements, lexicon, and scientific narrative) aligned with Therapeutic Areas for launch assets/disease area, including publication and medical education strategy and execution. About the Role Major Accountabilities: Leads the development, implementation, and dissemination…
Summary The Preclinical Safety (PCS) department within the Biomedical Research (BR) Translational Medicine Unit provides non clinical safety strategy of products in discovery, development and market, globally, with state of the art regulatory compliance. As a Scientific Study monitor, you…
Summary The Signatory Business Partner is accountable for ensuring promotional and non promotional materials and activities are fair, balanced and factually accurate and adhere to the ABPI code of practice and Novartis policies. Acts as a final medical signatory for…
Summary #LI Hybrid Location: London (The Westworks), United Kingdom (3 days per week on site) We are seeking a strategic and forward thinking Head of Regulatory Intelligence to lead our global efforts in monitoring and interpreting evolving regulatory landscapes. This…
Summary Location: London, United Kingdom or Dublin, Ireland Role Purpose: The Associate Clinical Development Director (Assoc. CDD) in Neurosciences provides input to development of protocols for assigned global clinical trials, scientific monitoring, and reporting of quality data. May be assigned…
Summary As our Clinical Development Director in Neurosciences you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. In addition, you may be responsible for the clinical and scientific…
Summary Novartis is deeply committed to transforming the lives of people living with blood cancers and life threatening blood disorders. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms,…
Job Description Summary We are seeking a highly motivated Associate Director of Biostatistics; you will be required to influence and drive the statistical strategy and innovation through strong collaborations and decision making for assigned trials/programs within (early/full) clinical development and/or…
Summary LI#Hybrid This position is based at the Westworks London office, with flexibility to work remotely two days a week. This position may require up to 5% travel as defined by the business. We are Clinical Sciences and Innovation at…
Summary #LI Hybrid (3 days per week on site) Location: London (The Westworks), United Kingdom Internal Job Title: International Program Regulatory Director Novartis is seeking an International Program Regulatory Director to join our dynamic team. The IPRD will play a…
Summary As a Strategy & Engagement Associate Director you wil drive strategic initiatives and deliverables that enhance GCO's strategy, engagement, operations, and organizational integration. You will also provide strategic partnership support to GCO Head and GCO Strategy office to position…
Summary The Precision Medicine Associate Director (PMaD) provides clinical drug development, scientific and technical expertise for successful implementation and execution of the Precision Medicine plans for clinical studies in a given program with a focus on ensuring timely execution to…
Summary The UK Therapy Area Medical Director for Solid Tumours is responsible for driving integrated medical affairs plans for pipeline, launch and marketed products in the Solid Tumour therapy area and developing and leading the medical TA team. About the…
Summary Novartis is deeply committed to transforming the lives of people living with blood cancers and life threatening blood disorders. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms,…
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. About…
Job Description Summary Are you passionate about advancing pharmaceutical research and ensuring drug safety at Novartis? The Preclinical Safety (PCS) department at Novartis BioMedical Research (BR) is seeking an experienced Genetic Toxicologist to join our dynamic team. More than 100,000…
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 currently looking for a Trial Vendor Senior Manager…
Summary Lead, develop and drive the execution of brand strategy or multiple brands plans (or new product launch readiness for Brand Lead–New Products role) to maximise market share and revenue growth for Novartis About the Role Major accountabilities: Develop strategic…
Summary Are you passionate about advancing pharmaceutical research and ensuring drug safety at Novartis? The Preclinical Safety (PCS) department at Novartis BioMedical Research (BR) is seeking an experienced Genetic Toxicologist to join our dynamic team. More than 100,000 people across…
Summary The Clinical Development Medical Director (CDMD) is the clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), or a large, complex trial, under the leadership of the (Sr.)…
Job Description Summary As part of International HEOR & PCO in International Value & Access, the Patient Centered Outcomes (PCO) HTA, TA Director within the HEOR TA teams, in partnership with HEOR leads co leads the PCO reimbursement strategy that…
Job Description Summary Oversees the provision of timely, high quality regulatory translations essential for product registration, maintenance, and launches worldwide.Job DescriptionKey RequirementsTeam leadership and strategic guidance Provides strategic guidance to a team composed of 5 6 direct reports and vendors,…
Job Description Summary Are you passionate about advancing pharmaceutical research and ensuring drug safety at Novartis? The Preclinical Safety (PCS) department at Novartis BioMedical Research (BR) is seeking an experienced Impurity Safety scientist to join our dynamic team.More than 100,000…
Summary As part of International HEOR & PCO in International Value & Access, the Patient Centered Outcomes (PCO) HTA, TA Director within the HEOR TA teams, in partnership with HEOR leads co leads the PCO reimbursement strategy that enables measurements…
Summary Location: Hybrid working 12 flexible days per month in the London office (The Westworks). #LI Hybrid About the role: As a member of our Global Talent Acquisition organization, you will be leading end to end recruitment and talent sourcing…
Summary Leads the strategic and operational planning and management of the assigned clinical program(s) from an end to end clinical operations perspective. Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To…
Summary LOCATION: London, UK ROLE TYPE: Hybrid Workig, #LI Hybrid As the Team Lead/Group Head of a team of PhDs/Postdocs focused on Clinical Research, you will be expected to people manage and develop this specialist group. You will also be…
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 Global…
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 for…
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 Affairs,…
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 building…
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 Documentation…
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 leader…
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 if…
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 providing…
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 our…
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 the…
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 less…
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 planning,…
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 have…
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 strategy…
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 for…
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. We…
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 Role Location:…
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 development…
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 role…
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, clinical…
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 science…
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. About…
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 clinical…
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 to provide…
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…