ABOUT THE ROLE: Join our Prague based team, which is changing the way how DHL Supply Chain works – from operations in warehouses to track&trace system for DHL Customers. Our team is currently looking for a Senior Consultant / Solution Designer, who will be responsible for consulting and designing web and mobile in-house developed IT solutions. YOUR PROFILE: • Consulting skills – high exposure to Product Owners based world-wide • Previous experience in designing in-house developed SW solution is a must - ideally both with Waterfall and Agile delivery methods • Strong analytical skills (UML - Use Case, Data Model, Process Model,
Please send your written application to Jakob Jan Verbraak directly. RAU | CONSULTANTS is not in charge of this search project.
Ability to foster positive relationships with external partners such as certification bodies, research institutes, and consultants. Fluent in English; Spanish or German language skills are a plus. At least 5 years of experience in a similar role. YOUR BENEFITS Nordex offers a range of attractive benefits – here’s a selection of what you can look forward to.
Ability to foster positive relationships with external partners such as certification bodies, research institutes, and consultants. Fluent in English; Spanish or German language skills are a plus. At least 5 years of experience in a similar role.
We are currently looking forHR Business Partnerwho will be closely cooperating with our MEA Accounting Competency Center department based in Phoenix, Mauritius. Would like to be a partner/ consultant advising on different HR disciplines to Managers and employees at local level? Are you interested to work in young fast growing environment with lots of new tasks in HR area?
Tieto Germany GmbH sucht in eine/n (Senior) SAP Reporting & Analytics Consultant (m/f/d) - Tieto Tech Consulting (ID-Nummer: 13664334)
Tieto Germany GmbH sucht in eine/n SAP S/4HANA Public Cloud Finance Consultant (m/f/d) [Full-time / part-time] - Tieto Tech Consulting (ID-Nummer: 13664330)
What makes you stand out You have a degree in economics, industrial engineering, data analytics or a comparable field.You have at least three years of professional experience in a comparable role, for example as a business analyst, strategy consultant or in controlling.You have experience in creating business cases and market analyses. You have very good knowledge of Excel, PowerPoint and BI tools such as Power BI, Tableau or SAP BW.You have an analytical and structured approach to your work and are innovative.You also have very good written and spoken German and English skills.
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.