KPMG AG Wirtschaftsprüfungsgesellschaft sucht in Düsseldorf, München, Berlin, Frankfurt, Hamburg, Stuttgart eine/n (Senior) Consultant SAP Planning & Analytics - Financial Services (w/m/d) (ID-Nummer: 13314431)
Einsatzort: Frankfurt am Main Start: 02.02.2026 | Laufzeit: bis 31.12.2026 | mit Option auf Verlängerung Arbeitszeit: 37,5 Stunden/Woche | Gleitzeit, Homeoffice nach Einarbeitung möglich Im Auftrag unseres Kunden, einem weltweit führenden Pharmaunternehmen, suchen wir Sie als: Customer Service / Supply Chain Specialist (m/w/d) – Logistik & Auftragsabwicklung Ihre Aufgaben Bearbeitung und Betreuung von Kundenaufträgen in verschiedenen SAP-Systemen (CEP, P08, PLE) für alle Export-Warenströme Durchführung von Bedarfsanalysen mit Supply-Planning-Tools (z.
Einsatzort: Frankfurt am Main Start: 02.02.2026 | Laufzeit: bis 31.12.2026 | mit Option auf Verlängerung Arbeitszeit: 37,5 Stunden/Woche | Gleitzeit, Homeoffice nach Einarbeitung möglich Im Auftrag unseres Kunden, einem weltweit führenden Pharmaunternehmen, suchen wir Sie als: Customer Service / Supply Chain Specialist (m/w/d) – Logistik & Auftragsabwicklung Ihre Aufgaben Bearbeitung und Betreuung von Kundenaufträgen in verschiedenen SAP-Systemen (CEP, P08, PLE) für alle Export-Warenströme Durchführung von Bedarfsanalysen mit Supply-Planning-Tools (z.
DEKRA Arbeit GmbH, as part of DEKRA SE, is among the top 10 personnel service providers in Germany and one of the fastest-growing staffing companies in Europe. At currently more than 120 locations across Germany and Europe, we are committed to establishing flexible personnel solutions and positively shaping the regional labor market.
Key Responsibilities: Ensure all deliverables are inspection-ready and compliant with regulatory and internal guidelinesMaintain central planning for document writing and QC deliverablesProvide recommendations for process improvements to enhance collaboration between CPP and document service teamsDrive document shell creation, QC processes, and timeline management Skills & Experience: Strong experience in writing full CSR for Phase 1 clinical pharmacology studies.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region.
Ensure overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensure services are delivered per contract.Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to 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 analyze trial progress.