Hays AG
Hays AG
BERG Personalmanagement GmbH
COSMO CONSULT AG
Hays AG
Hays AG
Sirius Facilities GmbH
Rau Consultants GmbH
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prognum Automotive GmbH
Deutsche Post AG
Rau Consultants GmbH
BleckmannSchulze GmbH
BleckmannSchulze Gruppe
prognum Automotive GmbH
Deutsche Post AG
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.
Leybold GmbH
Deutsche Post AG
Deutsche Post AG
Rau Consultants GmbH
Rau Consultants GmbH
IQVIA Commercial GmbH & Co. OHG
Deutsche Post AG
Deutsche Post AG
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?
Deutsche Post AG
Deutsche Post AG
CHEPLAPHARM Arzneimittel GmbH
DKV EURO SERVICE GmbH + Co. KG
Deutsche Post AG
Deutsche Post AG
ABOUT YOU GmbH & Co. KG
Deutsche Post AG
IQVIA Commercial GmbH & Co. OHG
IQVIA Commercial GmbH & Co. OHG
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.
Deutsche Post AG
IQVIA Commercial GmbH & Co. OHG
CSL Behring GmbH
Deutsche Post AG
Deutsche Post AG
IQVIA Commercial GmbH & Co. OHG
IQVIA Commercial GmbH & Co. OHG
Hays AG
CSL Behring GmbH
Deutsche Post AG
DKV EURO SERVICE GmbH + Co. KG
Deutsche Post AG
Jones Lang LaSalle SE
Aliaxis Deutschland GmbH