Salaire moyen: CHF74 634 /annuel
Plus de statistiquesRecevoir les offres d'emploi par email
Les résultats de la recherche: 48 offres d'emploi
- ...clinical development and making a meaningful impact to patients We are looking for an experienced and visionary Clinical Development Medical Director (CDMD) to take the lead in driving the strategic planning and execution of our cutting-edge clinical programs In this...SuggéréEn aoûtAssurance-invalidité
- 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
- ...Gesundheitsbereich mitgestalten und Menschen mit Sinn und Empathie verbinden? Dann bist du bei uns genau richtig! Als Sales Consultant im Bereich Medical bei der Adecco Gruppe in Basel bist du täglich im Austausch mit Fachkräften, die das Rückgrat unseres Gesundheitssystems bilden –...SuggéréActivité indépendanteTravail de vacances
- 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.) GPCH....SuggéréAssurance-invalidité
- ...a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Role Purpose As the Global Head of Medical Affairs Operations...Suggéré
- Summary The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As CDMD in the Renal TA, you will have oversight...SuggéréAssurance-invalidité
- Summary As our Clinical Development Medical Director in our Immunology Development Unit you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. About the Role...SuggéréAssurance-invalidité
- Summary Are you a highly skilled and ambitious medical professional with a passion for research? If so, we have an exceptional opportunity for you! Novartis, a world-class pharmaceutical company, is seeking a Clinical Development Medical Director - Renal...Suggéré
- ...relevant Design History File (DHF) documents, ensuring high-quality device design and development ~ Contribute to all phases of medical device development: ideation, prototyping, piloting, and manufacturing transfer ~ Ensure components meet quality standards for...Suggéré
- ...decision making in assigned indications/program with oversight. Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables. Contribute to external engagement with consultants,...Suggéré
- ...will lead programs through the end-to-end development cycle to seek successful registration and market access. This includes all medical and scientific aspects of clinical trials, programs and studies from the design phase, through implementation and finalization to include...SuggéréTemporaire
- ...EPSG) Support preparation and scientific quality of safety board meetings, including Integrated Safety Assessment Board (ISAB) and Medical Safety Review Board (MSRB) Review and advise on mechanistic studies, Risk Management Plans, and safety signal action plans...SuggéréEmploi postdoc
- ...Collaborate with internal and external partners to ensure scientific rigor in study design and analysis. Build partnerships with medical societies, academic institutions, and other stakeholders for RWD research collaborations. Contribute to enterprise-wide...Suggéré
- ...accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed...Suggéré
- ...accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed...SuggéréTemporaire
- ...shaping data42’s vision for how semantics can transform the landscape of multimodal & multidimensional data utilization in the R&D and medical continuum. About the Role Major accountabilities: ~ Interface seamlessly with semantic experts across the company...
- ...accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed...
- ...Purpose of the role: Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful...Heures supplémentaires
- ...Novartis 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...
- Summary This role is to provide strategic medical guidance and lead the development of experimental oncology agents in the TCO portfolio, from the Phase of preclinical development, continuing through clinical First in Human and Phase 1b/2 studies. As a Clinical...
