
Most sponsored roles at NOVARTIS PHARMACEUTICALS UK LIMITED paid £80k+ in 2024 (74% of 27 workers sponsored).
Certificates of Sponsorship issued, grouped by role (SOC 2010) and salary band. Source: Home Office.
Summary Pricing Director (PD) will drive the development of launch and in-market pricing strategies that enable access for our products in partnership with relevant functions (TA, S&G, Access, HEOR, Policy, Finance, etc.). The role requires the right capabilities and the right mindset to drive collaboration, impact, and innovation to realize our short- and long-term goals to fulfill our vision. The PD is expected to be a thought leader and expert in assigned therapeutic/disease area(s) and a
Summary The Publications & Content Manager is accountable for the high‑quality execution and management of therapeutic-area–aligned publication plans and scientific content programs. About The Role The role focuses on developing globally applicable, compliant scientific content aligned to the Scientific Communications Platform (SCP), ensuring adherence to internal standards and external regulations such as Global Publication Practice (GPP). Key aspects of the role Own and deliver publication
Summary This role can be based in the following locations: Basel, Switzerland; East Hanover, NJ, United States; Westworks, London, United Kingdom; Dublin, Ireland, or Hyderabad, India. Please apply to the advertised position relevant to to your location. Full time, Hybrid, At Novartis, we are re imagining how clinical trials are designed, delivered, and scaled—placing digital, operational data and AI at the heart of execution. As Head of GCO Technology & AI, you will define and lead the end
Band Level 6 Job Description Summary #LI-Hybrid Location: London, UK We’re a team of smart, dedicated people united by a drive to achieve together. In this role, you will lead the legal strategy and governance for Value & Access (V&A) across international markets, covering pricing and reimbursement, market access, HTA, payer contracting, public procurement, and related policy. You will provide practical, solution-oriented advice in a fast-changing environment shaped by trade barriers, competit
Summary Employment Type: Full‑time | Regular, Hybrid, Location: London (The Westworks) or Dublin (NOCC) Novartis is unable to offer relocation support for this role: please only apply if the locations of Westworks, London or Dublin are accessible for you About The Role Novartis is seeking an experienced Vendor Alliance Lead Associate Director to lead strategic partnerships and vendor delivery across cardiac safety, cardiac disease and respiratory diagnostics within Global Clinical Operations (GC
Summary Creation of high-quality complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery. About The Role Major Activities Demonstrate a command of assigned therapeutic areas and expertise with assigned products. Research and write original content for publications activities (primary and review manuscripts,
Summary The Global Medical Affairs Director develops and implements strategic and operational TAs Global Medical Affairs programs, with a focus on innovative evidence and/or launch readiness and/or post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy addressing and delivering strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems -Provides expertise in the development
Summary LOCATION: London, Dublin, Barcelona ROLE TYPE: Hybrid Working, The Lead Central Monitor (Lead CM) supports the Central Monitoring Head to drive excellence in clinical trial monitoring by establishing and delivering a state-of-the-art Central Monitoring capability at Novartis in Global Clinical Operations (GCO). The Lead CM is responsible for managing a team of CMs, for developing central and site monitoring strategies, ensuring that the configuration of the CM platform aligns with strate
Summary Location: London, UK This role does not offer relocation or visa support so please only apply if you have the right to work in the UK and the office location is convenient for you. Come and join our team of dedicated and passionate lawyers, united by a shared commitment to achieve impactful outcomes together! You will provide strategic counsel and be a trusted business partner to colleagues within the Novartis UK organisation, working closely with key decision makers across the business.
Summary As a Director, Translational Medicine Expert (TME), Clinical Pharmacology (CP TME), you will serve as the primary medical and scientific leader for FiH and Clinical Pharmacology studies. You will partner closely with cross functional Clinical Pharmacology Trial Teams, project level TMEs, and CRO collaborators to ensure the highest standards of medical supervision, participant safety, and scientific quality. TM Clinical Pharmacology is a cross‑functional expert group responsible for the d
Summary Primary Location: Barcelona, Spain Other Locations: Dublin, Ireland; London, UK; Novartis aims to reimagine medicine by delivering exceptional customer experience and engagement, enabling more patients worldwide to benefit from our therapies. The International Field Engagement team within Customer & Launch Strategy (CLS) strengthens the performance of international field organizations by embedding, evolving, and measuring best-in-class execution standards and capabilities. The Direct
Summary LOCATION: London, UK or Dublin, Rep of Ireland ROLE TYPE: Hybrid Working, LI-Hybrid How do you turn complex data into insights that shape global healthcare decisions? This role offers the chance to lead evidence strategies that influence regulators, payers, clinicians, and patients worldwide. As Director of Evidence Generation, you will design and deliver interventional and non-interventional studies that demonstrate the value of innovative medicines. Your work will bridge scientific rig
Summary We have an exciting opportunity to join the team to work on one of our priority brands in Immunology, specifically Dermatology. This opportunity gives you the chance to develop your career whilst playing an important part of the success of a team that has already changed lives of many people requiring Dermatology treatment in Scotland. This is a one year contract. About The Role Location Please note this role requires the successful candidate to live on the territory in Scotland and have
Summary LOCATION: London or UK Homeworker, Dublin, Barcelona or Madrid ROLE TYPE: Hybrid Working, 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 of Global Clinical Team(s) (GCT) is accountable for the design, implementation, and execution of a clinical development program(s) to support decisio
Summary As a Director, Translational Medicine Expert (TME), Clinical Pharmacology (CP TME), you will serve as the primary medical and scientific leader for FiH and Clinical Pharmacology studies. You will partner closely with cross functional Clinical Pharmacology Trial Teams, project level TMEs, and CRO collaborators to ensure the highest standards of medical supervision, participant safety, and scientific quality. TM Clinical Pharmacology is a cross‑functional expert group responsible for the d
Summary Office Location: London (The Westworks), United Kingdom (12 days per month on-site if living within 50 miles to our London office) (if living beyond 50 miles to our London office) We’re looking for a seasoned regulatory expert to lead global strategy and execution for digital medical devices, including Digital Health Technologies (DHTs) and Software as a Medical Device (SaMD). This role drives regulatory direction across development, registration, and post-approval, ensuring timely, comp
Summary Office Location: London (The Westworks), United Kingdom (12 days per month on-site if living within 50 miles to our London office) (if living beyond 50 miles to our London office) We’re looking for a seasoned regulatory expert to lead global strategy and execution for digital medical devices, including Digital Health Technologies (DHTs) and Software as a Medical Device (SaMD). This role drives regulatory direction across development, registration, and post-approval, ensuring timely, comp
Summary The Head of Scientific Learning & Capability, is a strategic enterprise leader responsible for designing, building, and sustaining industry‑leading capabilities across International Medical Affairs (IMA). This role leads the Scientific Learning & Capability team, to strengthen scientific, functional, and execution capabilities across International, Regional, and Country medical teams. The Director defines and delivers a coherent learning strategy and curriculum that enhances indi
Summary The Facility Manager ensures a safe, efficient, and user friendly workplace by overseeing daily operations, maintenance, compliance, vendor management, and all workplace support services while coordinating closely with landlords and internal partners. They also lead space management, sustainability efforts, KPIs tracking, and deliver facility projects—including relocations and fit outs—while driving continuous improvement and resolving operational challenges through strong stakeholder co
Summary Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables. Complies with project / study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistica