We bring together sector expertise, global scale and local knowledge to design and manage supply chains from raw materials and manufacturing through to the delivery of finished goods and return services. And by seamlessly connecting local operations across the world we are able to deliver the future of global trade.
Das kannst du bei uns MACHEN: Übernimm die technische Leitung des Frontend‑Software‑Engineerings unserer Web‑Plattform – mit Fokus auf Enablement, Orientierung und Coaching im Team.Baue eine zentrale Frontend‑Expertise im Unternehmen auf und präge als fachlicher Nukleus unser zukünftiges Frontend‑Wissensmodell.Trage technische Verantwortung und arbeite zugleich stark hands‑on mit sehr hohem Anteil an Frontend‑Entwicklung.Unterstütze weniger erfahrene Kolleg*innen aktiv durch Mentoring, Pair Programming und konstruktives, wertschätzendes Feedback.Steuere und koordiniere externe Partner*innen und stelle eine gemeinsame technische Ausrichtung sicher.Verantworte die Implementierung über den gesamten Software‑Lebenszyklus – von Architekturentscheidungen über Entwicklung bis hin zu Betrieb und Weiterentwicklung.Analysiere, optimiere und entwickle unsere bestehende Frontend‑Codebase kontinuierlich weiter.Führe Code Reviews durch, etabliere Tests und agier als technischer Sparringpartner auf Augenhöhe.Arbeite eng mit Backend‑, Design‑ und App‑Teams zusammen – insbesondere bei der Weiterentwicklung unserer Component Library, unseres Design Systems sowie OpenAPI‑basierter TypeScript‑Generatoren.Stelle hohe Softwarequalität sicher, u. a. durch Tests, dokumentierte Architekturentscheidungen (z.
Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections Leading studies at an operational level Provide expert review and initiate methodology development work with regards to statistical standards and validation procedures Consult on operational/statistical/therapeutic area topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding Process: Leads the database lock and unblinding process for the statistical team Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules) Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for complex and/or integrated reports) Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data) Provide expert review of ADaM reviewers guide (ADRG) and metadata Perform senior biostatistical review (SBR) Produce or perform quality control review of sample size calculations for complex studies Requirements: Masters or PhD degree in Biostatistics or a related field with relevant experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development expertsExperience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge of SAS or RExcellent knowledge of CDISC Data Standards Superb communication and collaboration skills Independent and pro-active problem solving skills IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Who you are Expert PHP (Laravel): Deep track record in designing and building complex e-commerce middleware. Architectural Design: Proven ability to document and implement scalable integration patterns for enterprise systems (ERP, PIM, PSP). AWS & Infrastructure: Expertise in core services (EC2, ECS/EKS, SQS, Kafka) and Infrastructure as Code (Terraform).
Company description 💧 Aliaxis is a leading technology company that designs sustainable, easy to install, and innovative fluid management solutions. Over 15,000 people have selected to work for us in more than 40 countries, meeting our customers’ most demanding needs for pipes and fitting systems in building, infrastructure, industrial and agriculture sectors.