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- ...development, registration and launch preparation activities. Your responsibilities will include, but are not limited to: Designing, planning,... ...timely supply of drug substances (DS) and drug products (DP) intended for pre-clinical and clinical development as well as...Suggéré
- ...part of the global technical development organization, we are responsible for the research and development of the drug substance solid state... ...and crystal structure prediction . This project is intended to further evolve existing software solutions in the realms of...Suggéré
- Summary Responsible for the contractually defined execution of Facility Management services in the buildings, infrastructure and sites at Novartis Headquarters, CH, Basel Campus (65 buildings, approx. 8'500 employees), Rotkreuz and Geneva. Support to evaluate...SuggéréTemporaire
- ...experimental designs, statistical models, analysis and data exploration methodologies at the study or project level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative...Suggéré
- ...and external partners. About the Role Your Key Responsibilities: Provide global strategic pharmacometrics leadership for integrated... ...using NLME methods and its application in Dose-exposure-response analysis, population PK/PD modeling, disease progression...Suggéré
- ...stakeholders. The role includes periodic 24/7 on-call duty (approx. every 6-7 weeks) to manage technical alarms and coordinate incident response. In this multifaceted professional-level role, you will: Coordinate the planning and forecasting of REFM budgets and human...SuggéréTemporaire
- ...collaboration with teams and clients. How You’ll Make An Impact Architecture and Implementation: As a Data Architect, you are responsible for data platforms, data products, and the foundation of complex AI projects. You can explain your solutions clearly to different...Suggéréà domicileTravail à domicileHoraire flexible
- ...architypes (e.g., UK/CAN) and Budget Impact architypes (e.g., Italy/Spain) needs and feasibility. About the Role Key Responsibilities: Supporting the International Value and Access (V&A) TA Head, represent Access talent and topics with internal partners and...Suggéré
- ...functional team, the role helps bring science-driven stories to life and ensures they resonate across digital platforms. Key Responsibilities Newsletter Support Draft and edit copy for our global newsletters. Help improve opening and click-through rates by...Suggéré
- ...considering various solutions, and proactively anticipating potential obstacles before making informed decisions. Specific Responsibilities & Scope You identify, scope and lead research projects. You serve as a subject matter expert on psychometrics, research...Suggéré
- ...At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed...Suggéré
- ...Please note that to be considered for this role you must have the right to work in this location. Tasks & Responsibilities: Contributing to a therapeutic area community that comprises the larger Clinical Operations Community, and enables clinical...Suggéré
- ...only apply if the location is accessible for you. Key Responsibilities Monitor clinical safety data, literature, and case reports... ...aggregate and single-case data Contribute to regulatory responses and prepare safety data for health authority reviews Support...SuggéréEmploi postdoc
- ...will support the team by driving key digital initiatives and collaborating with stakeholders across IT and PT functions. Your responsibilities include: Work with IT and PT stakeholders to plan, execute, and sustain digital solutions. Help define and manage user requirements...Suggéré
- ...Please note that to be considered for this role you must have the right to work in this location or hold an EU passport. Responsibilities: Develop and execute integrated evidence strategies to support the value of medicines. Act as a thought leader and...Suggéré
- ...and make a real difference for patients worldwide. #Hybrid Location: Basel, Switzerland About the Role Key Responsibilities: Support the implementation of TA/product brand internal & external communications strategy in collaboration with range of...
- ...value of our in-market medicines through evidence. As an individual contributor in our RWD/Post-Launch pod, you will have a dual-responsibility role. First, you will be our strategic expert in Real-World Evidence (RWE). You will proactively identify evidence gaps...
- ...depth evaluation, originality or ingenuity. Work is varied, unique and substantially more complex in nature. Significant level of responsibility and independent work. May serve as a peer mentor and point of escalation for new or less experienced members of the team and...
- ...members of the Neurosciences group plan, execute, document, analyze and interpret experiments. About the Role Your responsibilities will include: Designing, conducting and protocolling independently in vivo studies with specific focus on neuroinflammatory...
- ...reasons, we can offer you the chance to do it on a global scale and play a real role in shaping our exciting journey. Key Responsibilities Client & Delivery Success Lead projects to deliver agreed scope, on time and within budget, at the promised level of...Remote jobHoraire flexible
- ...excellence into impactful market experiences through advanced technology and analytics solutions. About the Role Key Responsibilities: Operational Leadership: Lead a team of experts to drive efficient V&A delivery to International and markets. Lead...
- ...platform The Semantics Technologies Associate Director will Lead data42’s implementation of Semantics and Metadata standards and be responsible of their quality across all data processing pipelines (Pre-Clinical, Clinical, Omics & RWD) from ingest to making data accessible...
- ...projections, and allocation strategies for assigned trials and programs. #LI-Hybrid Location : Basel, Switzerland Responsibilities include but not limited to: ~Leading and conduct the end-to-end feasibility process in collaboration with the country...Assurance-invalidité
- ...to influence and advise senior leaders and their teams, including General Managers, Area Heads, and global leaders. Your main responsibilities are, but not limited to: Strategic Leadership: Lead the strategic development and implementation of a comprehensive learning...
- ...ein großes Land/eine Gruppe von Ländern oder verwaltet ein juristisches Sachgebiet weltweit About the Role Key Responsibilities: Assume responsibility and provide strategic advice for ex-US group material litigations, ensuring effective management...
- ...We are currently seeking a highly motivated individual to join our team as QC Analyst II. The successful candidate will be responsible for the execution of assigned tasks in our laboratory, ensuring compliance with cGxP regulations. The ideal candidate will have...ApprentissageHoraire flexible
- Summary The Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As...CDD
- ...every voice matters. The Position The Device & Packaging Development department within Roche Technical Development is responsible for the development and support of drug delivery devices for the product portfolio. Our activities span a range of engineering disciplines...
- ...generations to come. Join Roche, where every voice matters. The Position The Corporate Strategy team is a high-performing group responsible for building strategic expertise and excellence across Roche. We work collaboratively with strategy teams throughout various...
- ...performance About the Role Main activities Leadership / Team management: Leads a Pharmaceutical Development Team responsible for Pharmaceutical Development and/or Clinical Manufacturing and/or non GMP Operations. Contributes members to multiple product...