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- Summary Join Novartis and be a part of something extraordinary! You will have a profound impact as a Medical Safety Lead. You'll spearhead safety evaluations, collaborate with dynamic global teams, and craft regulatory strategies that not only protect patients...EmpfohlenPostdoc Stelle
- ...across the whole value chain from target assessment to on-market and beyond. This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Science function, which enables portfolio decisions through proactive and integrative...EmpfohlenTemporär
- ...purchasing guidelines, and booking incoming goods (GR) after consultation with internal clients. Assist with resolving issues related... ...other key areas of Business Operations CH, including Health, Safety, and Environment (HSE), administration, and asset coordination...EmpfohlenTemporär
- ...to maximize productivity. Upholding high standards of laboratory and process safety. Co-authoring documentation required for process transfer to pilot plants. Acting as a consultant for troubleshooting during manufacturing campaigns. What you’ll bring to...Empfohlen
- ...into drug development plans across all phases and answering challenging questions on dose and regimen justification, study design, safety analysis among others Track record of contributions to external whitepapers/ policy shaping best practice in pharmacometrics. Internally...Empfohlen
- ...research projects, including publications. Cross-functional experience with clinical development, market access, HEOR, medical, safety, and regulatory teams. Strong leadership, communication, and organizational skills. Ability to manage change, inspire teams,...Empfohlen
- ...regional/country medical associates, where applicable Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall...EmpfohlenInvalidenversicherung
- ...and grow high-performing delivery teams across disciplines. Promote a healthy project culture, team engagement, and psychological safety. Provide performance feedback and support development plans for Zuhlke employees. Mentor junior Delivery Managers and foster...EmpfohlenRemote jobFlexible Arbeitszeit
- ...standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) Drive execution of the section of the program in partnership...EmpfohlenInvalidenversicherung
- ...data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead • Supporting (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section and may be a core member of the Safety Management Team, supporting overall program safety...EmpfohlenCDD
- ...concepts like traceability, transparency, reproducibility, and measurability in complex project and technology environments. Consulting: You view AI and data technologies as tools for tackling the challenges of digital transformation and help clients understand their...EmpfohlenVon zu HauseHomeofficeFlexible Arbeitszeit
- ...statistical analysis plan, reporting activities. Contribute to planning and execution of statistical analyses and statistical consultation within your cross-functional teams. Initiate, drive and implement novel methods and innovative trial designs in alignment...Empfohlen
- ...projects. Lead research projects end to end from design to implementation and communication of insights to stakeholders. Consultation Articulate complex ideas clearly, utilizing diverse communication channels and presentation techniques to effectively engage...Empfohlen
- ...Innovation: Explore and implement innovative technologies, including automation, to enhance efficiency in daily tasks. Radiation Safety: Adhere to radiation safety guidelines, including training, dosimetry monitoring, and proper handling and disposal of radioactive...EmpfohlenVollzeitLehrstelleFlexible Arbeitszeit
- ...You have at least 5 years of relevant experience in the pharmaceutical industry, a health technology assessment agency, or a consultancy. Your experience includes hands-on work in all of the following areas: Designing and implementing RWE studies for market...Empfohlen
- ...intermediates, and final products (API and DP) at all stages of process development. Conduct work in compliance with cGMP where applicable, safety, and regulatory requirements. Plan and document experiments/results independently and prepare for regulatory submissions such as...Soforteinstellung
- ...standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) • Drive execution of the section of the program in partnership...Invalidenversicherung
- ...TPP. Supports registration, market access, commercialization, and maintenance of product licenses (e.g., Core Data Sheet, Periodic Safety Update Report, clinical benefit-risk assessment for license renewals) for the compound(s) Together with Patient Safety, ensures continuous...Remote jobInvalidenversicherung
- ...regional/country medical associates, where applicable Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall...Invalidenversicherung
- ...related and are a Certified Internal Auditor (CIA). You possess 5 to 10 years of experience as an internal auditor or strategic consultant, preferably with a 'Big Four' firm or in the healthcare industry coupled with comprehensive knowledge of processes and risks either...
- ...process. Successfully compete clinical trial protocols, investigator brochures, and informed consent forms. Determine appropriate safety monitoring and risk management strategies. Ensure compliance with all applicable regulatory and ethical guidelines....
- ...at the forefront of shaping Roche's Pharma strategy through market and customer-centric insights. This team functions as internal consultants and strategists, partnering with commercial and cross-functional leaders, integrating data to activate insights-driven problem-...
- ...tailoring the drug, its dose and dosing regimen in such way to the patient that the clinical response is optimal in terms of efficacy and safety. We focus from identification of drug targets (molecular pathways relevant to disease) up to the completion of Proof of Concept...
- ...dedicated Laboratory Technician to join our in vivo research team, focusing on rodent and rabbit studies in the fields of toxicology, safety, efficacy, and pharmacokinetics/pharmacodynamics (PK/PD). Your responsibilities will include: Participating in in vivo...TemporärInvalidenversicherung
- ...art analytical science, technologies and processes. Working according to appropriate SOPs, GMP, Quality Directives, Health and Safety & internal Novartis guidelines. In order to successfully fulfill this role the analytical expert should bring the following qualifications...
- ...Join Our Team of Enthusiasts! At KVALITO Consulting Group, a women-owned business founded in 2013, we are dedicated to transforming the life sciences and healthcare sectors through tailored, innovative solutions that prioritize quality and people. Guided by our vision...VollzeitIm AugustLehrstelle
- ...will encourage you to come with your own ideas and suggestions. To this end, you may also interact with experts outside the team and consult the scientific literature. Who you are: You are a Master student (or you graduated within 12 months prior to the start date...