bei der Analyse, Konzeption und Implementierung unseres Data WarehouseSie implementieren standardisierte Reports auf Basis fachlicher Anforderungen und begleiten Kollegen aus unterschiedlichen Fachbereichen
evaluations and reports of your results and provide clear decision templates to management.You accompany the introduction of new developments into mass production at our international manufacturing sites and
-quality evaluations and reports of your results and provide clear decision templates to management.You accompany the introduction of new developments into mass production at our international manufacturing
unserer Analysen, Reports und Datenkorrelationen in unserem CRM / Marketing Automation System für verschiedenste Datenströme Du verantwortest die Visualisierung deiner aufbereiteten Insights
environment by learning and adopting best practices. Follow and adhere to safety and security policies and procedures. Report immediately any safety or security issues or concerns. Your profile: Degree
study. Good Exposure and have worked on Define.xml and package creation, worked on Pinnacle reports Develop and validate on TLF'S without any support. should have good first-hand experience on Tables and
navigation payload and satellite levels test specifications Analysis of requirements coverage and derivation of verification close-outs Contribution to test reports Contribute to development of SOCs / RVM
statistical reports. Requirements: BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory
plus.Minimum 5 years’ experience managing complex ER cases including investigations, ill-health, dismissals, appeals, and report writing.Experience of a fast-paced matrixed organization is helpful.Training
Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study
regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending on client model there might
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form
Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study
ensure that target enrollment will be met across the allocated countries.Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to
in business development activities for target clients and contribute to advancing JLL's market position in sustainability.Regularly report on progress to the Head of Sustainability - EMEA Markets Advisory and
suitable positions and projects. Supporting Pharmacovigilance activities including input to safety reports (local PSURs) Review and approval of promotional and non-promotional externally focused materials
suitable positions and projects. Supporting Pharmacovigilance activities including input to safety reports (local PSURs) Review and approval of promotional and non-promotional externally focused materials
/ savings from tenders / process re-design / negotiation initiatives and provide monthly/ Quarterly reports to Sourcing & Procurement LeadershipTo ensure that all vendor details and files are complete and
procedures and create test result reports Improve existing designs with the help of real time, static timing and post layout simulations Your profile: Completed studies in Engineering or similar First
their clients, passionate about performance and commitment to a better future. Core Responsibilities The Assistant Facilities Manager (AFM), who reports into the EMEA SFM should be capable of managing
Opening of project WBS Project controlling; Cost statement / report preparation (incl audit certificate) Invoicing / Cash allocation Revenue / Grant recognition -> as input to accounting for closing process
Opening of project WBS Project controlling; Cost statement / report preparation (incl audit certificate) Invoicing / Cash allocation Revenue / Grant recognition -> as input to accounting for closing process
risk assessment requirementsPrepare and assist in the preparation of monthly reports, provide inputs for the finalization the yearlyEnd to end finance admin of PO’s, invoices, and trackersSupplier
analysis of market trends, technological advancements, and competitor activities. Prepare comprehensive reports outlining findings and recommendations to inform strategic decision-making processes. Regularly
und Nachhalten von Kennzahlen mit abteilungsübergreifenden Fachbereichen Abzug von Daten aus zentralen Quellen, Datenbanken und Reports zur weiten Analysevorbereitung und -verarbeitung Unterstützung
interpreting experimental data and contributing to technical reports and presentations You have the following skills and qualifications: You are a registered student in aerospace engineering, material science
you make the most of yours. Achieve your ambitions – join us at JLL! Role Purpose The Project Coordinator Moves reports to the Senior Facilities Manager. His/her main function is to coordinate the
are aligned with the client you’ll be supporting to drive sustainability through everything that we do, across all service lines, operations, and job positions. What this job involves Report to the