Jobs from Novartis

Job Description Summary LI-Hybrid For Hybrid working there is an expectation of 12 days per month onsite. This role can also be provided on a Remote working basis, subject to eligibility criteria. Eligibility for remote work can be discussed at interview stage. Location: Westworks, London, UK Other Locations: Dublin, Ireland. Please apply to the Dublin advertisement for this location This role is

Band Level 4 Job Description Summary LI-Hybrid Location: London, UK. Assigned therapeutic area: CRM This role is based in London, UK. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. The Senior Scientific Writer II develops high quality, accurate, and compliant medical and scientific communications aligned with therapeutic area

Band Level 6 Job Description Summary The Senior Clinical Development Medical Director (Sr CDMD) will lead the end-to-end strategy and execution of assigned renal clinical development program(s) across the full Research, Development and Commercial (RDC) continuum; from early development through pivotal/registrational phases. This is a key leadership role requiring hands-on experience in both early

Job Description Summary LI-Hybrid Location: London, UK This role is based in London, UK. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. The Senior Scientific Engagement & Program Manager, part of the International Medical Affairs, Center of Excellence (IMACE) Scientific Operations team. Responsible for planning, coordinating,

Job Description Summary The Clinical Development Director (CDD) is the clinical/scientific expert and if assigned the clinical development lead of a section of a global clinical program and/or trial. (e.g., an indication, a new formulation, or a specific development phase) or a large, complex trial, under the leadership of the GPCH. The CDD may be assigned to have a team leadership role for sectio

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 of 1-year duration, within two different RA functions. Job Description Are you interested t

Job Description Summary Ready to shape the future of oncology on a global scale? As Head, Global Medical Affairs Oncology, you will lead the integrated medical strategy across the product lifecycle - bringing scientific leadership into early portfolio decisions, strengthening the global medical voice in late-stage development, and ensuring evidence plans meet real stakeholder needs. This is a high

Job Description Summary The Risk-Based Quality Management (RBQM) Risk surveillance Lead is responsible driving the adoption of RBQM practice at trial level and oversee the implementation, and continuous improvement. Risk Surveillance Lead works within a matrix environment and has overall account-ability for the surveillance of the quality risks across the assigned trials and program, enabling a co

Job Description Summary The Senior Clinical Development Medical Director (Sr CDMD) will lead the end-to-end strategy and execution of assigned renal clinical development program(s) across the full Research, Development and Commercial (RDC) continuum; from early development through pivotal/registrational phases. This is a key leadership role requiring hands-on experience in both early and late phas

Job Description Summary LI-Hybrid (12 days per month on-site if living within 50 miles of our London office) LI-Remote (Homeworker if living further than 50 miles of our London office) Office Location: London (The Westworks), United Kingdom We are looking for a Global Labelling Manager, Content to support the development and delivery of high-quality global labelling for our products. In this role,

Band Level 5 Job Description Summary LOCATION: Homeworking UK or Ireland or Hybrid Working at Westworks London or Dublin: Please apply only if any of these locations are accessible to you, as relocation support is not available. ROLE TYPE: Homeworking, LI-Home or Hybrid working, LI-Hybrid As a core member of the Clinical Trial Team (CTT), the main purpose of this position is accountability for ven

Job Description Summary Location: Westworks, London, UK Full time, Hybrid, LI-Hybrid As the study’s start-up linchpin subject matter expert for eCOA and Translations, the Vendor Start-Up Manager ensures vendors are fully aligned, validated, and ready to deliver—protecting timelines, quality, and patient experience from protocol finalisation through database go-live. Job Description Reporting to th

Job Description Summary As Associate 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, p

Job Description Summary Ready to shape how medical evidence influences patient care on a global scale? As Associate Director, Global Medical Affairs Study Management, you will lead the end to end delivery of high impact medical studies across a Neuroscience disease area portfolio. This is a strategic, hands on role where scientific insight meets operational leadership - driving non interventional

Job Description Summary Office Location: London (The Westworks), United Kingdom LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office) LI-Remote Remote (if living beyond 50 miles to our London office) Internal Job Title: Global Program Regulatory Associate Director We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Card

Band Level 7 Job Description Summary LOCATION: London or UK Homeworker, Dublin, Barcelona or Madrid ROLE TYPE: Hybrid Working, LI-Hybrid 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

Job Description Summary Employment Type: Full‑time | Regular, Hybrid, LI-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 partnership

Job Description Summary LOCATION: London, Dublin, Barcelona ROLE TYPE: Hybrid Working, LI-Hybrid 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

Job Description Summary As a Senior* Clinical Development Medical Director, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. The Senior/Clinical Development Medical Director (CDMD) is the clinical leader of defined program level activities (e.g., submission activities, briefing books, clinical study

Job Description Summary Location: Westworks, London, UK; Dublin, Ireland or Barcelona, Spain Full time, Hybrid, LI-Hybrid Please note that we can only consider candidates who are based on the above locations or in commutable distances to our office locations. 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