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- ...Switzerland. Novartis is unable to offer relocation support: please only apply if accessible. Are you ready to shape the future of regulatory precision medicine? As a Regulatory Diagnostics Senior Manager at Novartis, you’ll play a pivotal role in advancing our...Suggéré
- Summary LOCATION: Basel, Switzerland ROLE TYPE: Hybrid working, #LI-Hybrid The Global Medical Affairs Executive Director Remibrutinib acts as enterprise medical voice for Remibrutinib and the associated indications/disease areas across the full lifecycle...Suggéré
- ...worked to support the passage of numerous bills that have benefitted close to 500 million people in developing countries. Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy. This is a part-time 12-hours per...SuggéréTravail à distanceTemps partielRemote job
- ...Authorities. The opportunity: In this role you will have considerable cross-functional interaction, notably including QA, Regulatory Affairs, Clinical and Commercial functions. This role reports to the Section Head of Device Engineering and is integrated into the...Suggéré
- ...clinical development program(s) to support decision milestones, regulatory requirements and market access. The GCPH may contribute to... ...stakeholders (e.g., Research, Translational Medicine, Global Medical Affairs (GMA), Marketing, Health Economics & Outcomes Research), and...SuggéréRemote jobAssurance-invalidité
- ...maturity according to RA business objectives. The Capability Lead will drive the Centralized Data Quality Management culture in Regulatory Affairs and ensure Data Quality consistency, correctness and completeness across all applicable RA systems and platforms. About the...Suggéré
- ...Integration requirements. This role requires a deep understanding of regulatory data and how it flows through systems across the regulatory... ...and Data Integrations landscape of pharmaceutical regulatory affairs and Regulatory Information Management ~ Practical experience...Suggéré
- ...will collaborate with cross-functional teams across the drug development value chain, including research and early development, regulatory affairs, data sciences, and biomarkers, to ensure efficient decision-making and successful progression of treatments through the...SuggéréAssurance-invaliditéHoraire flexible
- ...such as liaising on behalf of Novartis Biomedical Research with regulatory authorities, accreditation bodies, and external groups and... ...in 3Rs Granting program Together with colleagues in Public Affairs, promote openness and education about the continued need for and...Suggéré
- ...DA Access team, strategically and operationally, across the R-D-C continuum, working in partnership with strategic CLS DAs, Medical Affairs, and our Novartis Regions and priority Country teams to maximize access to IM assets. Develop and implement transformative...Suggéré
- ...Therapeutic Areas (TAs). You’ll help bring our integrated TA strategy to life—spanning communications, patient advocacy, and public affairs — by supporting launch excellence and delivering high-impact, above-brand and priority brand initiatives. Your work will empower...Suggéré
- ...pharmaceutical facilities and maintenance environment. Knowledge and understanding of Good Laboratory Practices (GLP) and other regulatory regulations regarding facility operations. Business - High level of facility/utility operations and the ability to understand...SuggéréTemporaire
- ...and implement novel methods and innovative trial designs in alignment with the Lead Statistician. Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight. Collaborate...Suggéré
- ...incumbent will closely partner with Top International (Int) markets and Regions, and together with Value & Access (V&A), Int Medical Affairs (IMA), Launch Excellence & Execution (LE&E), Customer & Market Activation (CMA), Int Business Operations, Patient Engagement and...SuggéréHeures supplémentaires
- ...in appropriate fora and organizations to drive the Novartis strategic access agenda. • Collaborate and partner with TAs, Medical Affairs, Development and Biomedical Research to enhance the value proposition, access strategy and access-relevant evidence packages. • With...Suggéré
- ...You will oversee contamination testing, cell line authentication, and advanced QC processes while ensuring adherence to SOPs, regulatory guidelines, and ethical standards for stem cell and organoid research; You will develop and standardize protocols for isolating...
- ...related disciplines for evidence generation. Strong understanding of drug development and ability to deliver impactful evidence for regulatory, market access, and clinical adoption. Experience with research methodologies, statistical methods, and observational/...
- ...in the assigned project or section of a clinical program Leading development of clinical sections of trial and program level regulatory documents Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions,...Assurance-invalidité
- ...identify trends and patterns, and implement analysis pipelines. Develop AI solutions to resolve issues for our partners (e.g., Quality, Regulatory, Manufacturing). Junior Technical Lead: As a Junior Technical Lead, you will support the team by driving key digital...
- ...strong external network, build policy partnerships and coalitions as required. Provide policy thought leadership for Global Public Affairs led engagements that support healthcare system and policy change conducive to the Novartis portfolio. What you’ll bring to the...
