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- Data Scientist
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- Medical advisor
- Clinical Affairs Manager
- Medical Affairs
- Clinical Data Manager
- Case Management
- Clinical Data Associate
Standorte
- München
- Stuttgart
- Nürnberg
- Karlsruhe
- Mannheim
- Augsburg
- Freiburg im Breisgau
- Ulm
- Baden-Baden
- Würzburg
- Regensburg
- Heilbronn
- Heidelberg
- Pforzheim
- Ingolstadt
- Reutlingen
- Erlangen
- Bayreuth
- Oberkochen
- Walldorf, Baden-Württemberg
- Europa
- Westliches Europa
- Süddeutschland
- Bayern
- Baden-Württemberg
- Neckarland-Schwaben
- Südbayern
- Schwarzwald
- Oberbayern
- Ostbayern
- Nordbayern
- Franken
- Nordbaden
18.200 Treffer für Clinical Data Management Jobs in Süddeutschland im Umkreis von 30 km
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Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Actual position's title: Clinical Data * Participating
Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Actual position's title: Clinical Data * Participating
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Develop IRT System specifications to meet the needs of the study design in collaboration with Clinical Trial Supply Unit (CTSU) functions, Medical, Clinical Data Management and Biostatistics * Support the successful setup of the supply chain and patient management activities through the use of IRT * Exhibit ability to interpret complex project requirements and provide ability to interpret highly complex experimental data and project requirements * Solid project management skills including presenting projects and status reports to different audiences
Develop IRT System specifications to meet the needs of the study design in collaboration with Clinical Trial Supply Unit (CTSU) functions, Medical, Clinical Data Management and Biostatistics * Support the successful setup of the supply chain and patient management activities through the use of IRT * Exhibit ability to interpret complex project requirements and provide ability to interpret highly complex experimental data and project requirements * Solid project management skills including presenting projects and status reports to different audiences
Noch nichts dabei? Es gibt 18198 weitere Jobs, die zu deiner Suche passen könnten
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Clinical Study Project Management: Take full responsibility for clinical trials in the role as sponsor and of non-interventional healthcare studies in fully outsourced model, steering scope, timelines and budget while safeguarding patient safety and data integrity. * Experience: Professional experience in clinical research project management (pharmaceutical industry or contract research organization) are an asset, but we are also open for structured and well-organized graduates. Department Clinical Research - The Clinical Research team is responsible for the implementation of all clinical research projects, from planning to reporting. Projects comprise clinical trials as well as all types of non-inter
Clinical Study Project Management: Take full responsibility for clinical trials in the role as sponsor and of non-interventional healthcare studies in fully outsourced model, steering scope, timelines and budget while safeguarding patient safety and data integrity. * Experience: Professional experience in clinical research project management (pharmaceutical industry or contract research organization) are an asset, but we are also open for structured and well-organized graduates. Department Clinical Research - The Clinical Research team is responsible for the implementation of all clinical research projects, from planning to reporting. Projects comprise clinical trials as well as all types of non-inter
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You will be responsible for defining, planning, and executing all necessary clinical studies and projects worldwide and evaluating clinical data for product definition, registration, and marketing purposes. * Responsibility for budget and timeline planning for the entire clinical strategy Oversight of statistical analysis and evaluation of clinical data Your Role As a Clinical Affairs Manager (m/f/x), you will play a pivotal role in driving the clinical strategy for the international approval of complex new product developments and product improvements in the ZEISS microsurgery. * Definition and implementation of the clinical evaluation strategy for complex and challenging development projects focused on innovative mi
You will be responsible for defining, planning, and executing all necessary clinical studies and projects worldwide and evaluating clinical data for product definition, registration, and marketing purposes. * Responsibility for budget and timeline planning for the entire clinical strategy Oversight of statistical analysis and evaluation of clinical data Your Role As a Clinical Affairs Manager (m/f/x), you will play a pivotal role in driving the clinical strategy for the international approval of complex new product developments and product improvements in the ZEISS microsurgery. * Definition and implementation of the clinical evaluation strategy for complex and challenging development projects focused on innovative mi
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The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. Accordingly, the candidate is responsible for executing the technology transfer in accordance with the established standard processes to facilitate alignment of tech transfer and validation activities across the projects for Drug Product manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a smooth transition of projects, recommends, and implements new technologies, as needed and supports Supply Chain Management with technical issues during ...
The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. Accordingly, the candidate is responsible for executing the technology transfer in accordance with the established standard processes to facilitate alignment of tech transfer and validation activities across the projects for Drug Product manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a smooth transition of projects, recommends, and implements new technologies, as needed and supports Supply Chain Management with technical issues during ...
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Scientific Project Manager for Governance & Regulatory Processes
Scientific Project Manager for Governance & Regulatory Processes
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
Experience with bioinformatics, research data management, or handling sensitive human or clinical data is strongly preferred - We are seeking a scientific project manager to support the GHGA office in coordinating GHGA's multi-stakeholder activities, with a focus on governance, grant management, regulatory workflows, and legal processes related to data access and operation of the GHGA. We welcome applicants with diverse academic and professional backgrounds that intersect with project management, data governance, research infrastructure, or regulatory processes. * Demonstrated experience in science and project management, research administration, regulatory affairs and legal management, and data governance, ideally within an academic environment - The German Cancer Research Center coordinates the German Human Genome-Phenome Archive (GHGA), a national research data ...
Experience with bioinformatics, research data management, or handling sensitive human or clinical data is strongly preferred - We are seeking a scientific project manager to support the GHGA office in coordinating GHGA's multi-stakeholder activities, with a focus on governance, grant management, regulatory workflows, and legal processes related to data access and operation of the GHGA. We welcome applicants with diverse academic and professional backgrounds that intersect with project management, data governance, research infrastructure, or regulatory processes. * Demonstrated experience in science and project management, research administration, regulatory affairs and legal management, and data governance, ideally within an academic environment - The German Cancer Research Center coordinates the German Human Genome-Phenome Archive (GHGA), a national research data ...
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Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) Sie agieren als zentrale Steuerungs- und Integrationsfunktion zwischen R&D, Produktmanagement, CPO, CTO sowie weiteren internen und externen Stakeholdern. * Enge Zusammenarbeit mit Produktmanagement und CPO zur Sicherstellung konsistenter Projekt-, Produkt- und Technologieziele * Einführung, Skalierung und Weiterentwicklung von Jira Premium als zentrales Projekt- und Portfoliomanagement-Tool * Mehrjährige (Senior-)Erfahrung im Projektmanagement komplexer Entwicklungs- oder Softwareprojekte, idealerweise im MedTech- oder regulierten Umfeld * Sehr gutes Verständnis klassischer und agiler Projektmanagement-Methoden (z. B. Scrum, SAFe-nahe Ansätz
Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) Sie agieren als zentrale Steuerungs- und Integrationsfunktion zwischen R&D, Produktmanagement, CPO, CTO sowie weiteren internen und externen Stakeholdern. * Enge Zusammenarbeit mit Produktmanagement und CPO zur Sicherstellung konsistenter Projekt-, Produkt- und Technologieziele * Einführung, Skalierung und Weiterentwicklung von Jira Premium als zentrales Projekt- und Portfoliomanagement-Tool * Mehrjährige (Senior-)Erfahrung im Projektmanagement komplexer Entwicklungs- oder Softwareprojekte, idealerweise im MedTech- oder regulierten Umfeld * Sehr gutes Verständnis klassischer und agiler Projektmanagement-Methoden (z. B. Scrum, SAFe-nahe Ansätz
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You will shape the direction of global clinical safety, medical affairs, and pharmacovigilance - ensuring the highest standards of patient safety and scientific integrity across our vaccine portfolio. We're looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manu
You will shape the direction of global clinical safety, medical affairs, and pharmacovigilance - ensuring the highest standards of patient safety and scientific integrity across our vaccine portfolio. We're looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manu
It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. As a Senior Software Developer for FORUM, you are designing and developing a key health data management product for ophthalmology. You define and implement business features, technical enablers, and security concepts for a complex data management solution which runs on-Prem and in cloud. * Servant leader for java development, especially for health data management platforms - ZEISS Medical Ecosystem opens possibilities for the creation of new solutions, where data passes seamlessly from one ZEISS devi
It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. As a Senior Software Developer for FORUM, you are designing and developing a key health data management product for ophthalmology. You define and implement business features, technical enablers, and security concepts for a complex data management solution which runs on-Prem and in cloud. * Servant leader for java development, especially for health data management platforms - ZEISS Medical Ecosystem opens possibilities for the creation of new solutions, where data passes seamlessly from one ZEISS devi
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(Senior) Product Support Specialist – Cranial & Functional Planning Applications
(Senior) Product Support Specialist – Cranial & Functional Planning Applications
Brainlab
München
Teilweise Home-Office
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. * Experience with medical image data stored in DICOM (Digital Imaging and Communications in Medicine) standard
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. * Experience with medical image data stored in DICOM (Digital Imaging and Communications in Medicine) standard
The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * End to end electronic Trial Master File (eTMF) set-up and
The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * End to end electronic Trial Master File (eTMF) set-up and
Build proof-of-principle demonstrators & test your solution with product management and our clinical partners * Evaluate and refine your approach on real-world data
Build proof-of-principle demonstrators & test your solution with product management and our clinical partners * Evaluate and refine your approach on real-world data
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As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. * Analyze logistics data to identify areas for process improvement and implement new efficiencies. * Bachelor's degree in Supply Chain Management, Logistics, or a related field.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. * Analyze logistics data to identify areas for process improvement and implement new efficiencies. * Bachelor's degree in Supply Chain Management, Logistics, or a related field.
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The role requires expertise in clinical trial design, medical data interpretation, and regulatory compliance, with a strong focus on patient safety, risk mitigation, and adherence to study protocols. * Assist in the review and interpretation of clinical trial data, ensuring accuracy and relevance. * Knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials * Ability to interpret clinical trial data, assess safety trends, and make informed medical decisions. * Ability to review and interpret clinical data, protocols, and study reports. * Analytical and critical thinking to assess and interpret clinical data effectively. The Medical Monitor is a key clinical expert responsible for ensuring the medical and scientific integrity of clinical trials, overseeing patient safety, and supporting study teams in protocol execution.
The role requires expertise in clinical trial design, medical data interpretation, and regulatory compliance, with a strong focus on patient safety, risk mitigation, and adherence to study protocols. * Assist in the review and interpretation of clinical trial data, ensuring accuracy and relevance. * Knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials * Ability to interpret clinical trial data, assess safety trends, and make informed medical decisions. * Ability to review and interpret clinical data, protocols, and study reports. * Analytical and critical thinking to assess and interpret clinical data effectively. The Medical Monitor is a key clinical expert responsible for ensuring the medical and scientific integrity of clinical trials, overseeing patient safety, and supporting study teams in protocol execution.
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Medical Science Liaison Manager, Neurology, Northern Germany, fixed-term until April 2027
Medical Science Liaison Manager, Neurology, Northern Germany, fixed-term until April 2027
Alexion Pharma Germany GmbH
Germany - Munich
The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives * Ensure timely and informative scientific/medical exchanges with external customers and internal , which accurately reflect scientific data, in accordance with compliance policies and procedures as well as with legal and ethical standards * Lead the implementation of medical affairs practices to assess new indications, the treating community, patient pathways, diagnostic practices and management strategies in relevant disease areas * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries
The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives * Ensure timely and informative scientific/medical exchanges with external customers and internal , which accurately reflect scientific data, in accordance with compliance policies and procedures as well as with legal and ethical standards * Lead the implementation of medical affairs practices to assess new indications, the treating community, patient pathways, diagnostic practices and management strategies in relevant disease areas * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries
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You will directly contribute to Custom Surgical's mission by enabling robust data capture, smooth clinical workflows, and seamless integration between mobile devices, hardware, and cloud systems. You will work on mobile software used daily in clinical environments, where reliability, performance, and efficiency are critical. * Handle large volumes of data efficiently, both locally on-device and over networks; This role requires deep hands-on experience with Swift and Kotlin, solid engineering fundamentals, and the ability to work close to hardware, imaging, and data-heavy workflows. * Solid understanding of mobile app architecture and lifecycle management; * Direct impact on products used in real clinical environments worldwide;
You will directly contribute to Custom Surgical's mission by enabling robust data capture, smooth clinical workflows, and seamless integration between mobile devices, hardware, and cloud systems. You will work on mobile software used daily in clinical environments, where reliability, performance, and efficiency are critical. * Handle large volumes of data efficiently, both locally on-device and over networks; This role requires deep hands-on experience with Swift and Kotlin, solid engineering fundamentals, and the ability to work close to hardware, imaging, and data-heavy workflows. * Solid understanding of mobile app architecture and lifecycle management; * Direct impact on products used in real clinical environments worldwide;
The Associate Director Sales Amyloidosis will be in charge of effectively managing the team of and drive key account management, sales performance and flawless execution within the assigned area. * Show high expertise in corrective counseling and performance improvement management * Ensure that all RAM activities are in accordance with Alexion's SOPs, compliance policy and data protection laws * Strong business, analytical and clinical acumen
The Associate Director Sales Amyloidosis will be in charge of effectively managing the team of and drive key account management, sales performance and flawless execution within the assigned area. * Show high expertise in corrective counseling and performance improvement management * Ensure that all RAM activities are in accordance with Alexion's SOPs, compliance policy and data protection laws * Strong business, analytical and clinical acumen
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Key Account Manager Neuroscience - North-West Germany
Key Account Manager Neuroscience - North-West Germany
Jazz Pharmaceuticals Germany GmbH München
München
Teilweise Home-Office
Position Jazz products effectively through scientific and clinical value. * Business Intelligence: Analyze territory trends and data to inform strategy, anticipate market changes, and adjust plans in real time. * The size of territory will necessitate appropriate management of travel requirements to ensure coverage of customers as directed by the management team * Exceptional account management capabilities and the ability to navigate and influence within complex customer environments – strategic, analytical, and relentlessly customer-focused.
Position Jazz products effectively through scientific and clinical value. * Business Intelligence: Analyze territory trends and data to inform strategy, anticipate market changes, and adjust plans in real time. * The size of territory will necessitate appropriate management of travel requirements to ensure coverage of customers as directed by the management team * Exceptional account management capabilities and the ability to navigate and influence within complex customer environments – strategic, analytical, and relentlessly customer-focused.
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This position reports to the Automation Clinical IT Innovations, Product and Program Management and is part of the Product Management/Marketing Team. * Translate user-centric service and product requirements into reusable platform capabilities such as IoT-based instrument connectivity, authentication, data management, predictive maintenance, analytics, and GenAI-powered workflows. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to
This position reports to the Automation Clinical IT Innovations, Product and Program Management and is part of the Product Management/Marketing Team. * Translate user-centric service and product requirements into reusable platform capabilities such as IoT-based instrument connectivity, authentication, data management, predictive maintenance, analytics, and GenAI-powered workflows. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to
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Clinical Application Specialist – Neurorehabilitation (m/w/d)
Clinical Application Specialist – Neurorehabilitation (m/w/d)
EGZOTECH SP Z O O
Region Süddeutschland
Teilweise Home-Office
Clinical Application Specialist – Neurorehabilitation * Klare Entwicklungs- und Karrieremöglichkeiten, z. B. Richtung Clinical Lead, Produkttrainer
Clinical Application Specialist – Neurorehabilitation * Klare Entwicklungs- und Karrieremöglichkeiten, z. B. Richtung Clinical Lead, Produkttrainer
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Sales Manager (m/w/d) Softwarelösungen - Infrastrukturmanagement & Smart City
Sales Manager (m/w/d) Softwarelösungen - Infrastrukturmanagement & Smart City
Barthauer Software GmbH
Süddeutschland, Home-Office
Teilweise Home-Office
Trendthemen wie Smart City, BIM, Data Mining, Augmented Reality, KI-gestützte Software-Tools oder Cloudlösungen setzen sie gemeinsam mit ihren Kunden in leistungsfähige Konzepte für ein nachhaltiges Ressourcenmanagement um. Zum Ausbau unseres Vertriebes suchen wir einen Sales Manager (m/w/d) für Softwarelösungen im Bereich Infrastrukturmanagement & Smart City in Süddeutschland (remote). * Vertrieb innovativer und markführender Softwarelösungen im Bereich Infrastrukturmanagement und Smart City
Trendthemen wie Smart City, BIM, Data Mining, Augmented Reality, KI-gestützte Software-Tools oder Cloudlösungen setzen sie gemeinsam mit ihren Kunden in leistungsfähige Konzepte für ein nachhaltiges Ressourcenmanagement um. Zum Ausbau unseres Vertriebes suchen wir einen Sales Manager (m/w/d) für Softwarelösungen im Bereich Infrastrukturmanagement & Smart City in Süddeutschland (remote). * Vertrieb innovativer und markführender Softwarelösungen im Bereich Infrastrukturmanagement und Smart City
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Global Head of Supply Chain Management (m|w|d)
Global Head of Supply Chain Management (m|w|d)
Kienbaum Consultants International GmbH
Süddeutschland
Teilweise Home-Office
Das Supply Chain Management nimmt dabei eine zentrale Rolle ein. * Stärkung und Weiterentwicklung einer robusten, zukunftssicheren und belastbaren Supply Chain, einschließlich Risikomanagement, Business Continuity und präventiver Stabilisierung kritischer Wertschöpfungsstufen * Einsatz moderner KPI- und Performance-Management-Methoden zur wirksamen Steuerung und kontinuierlichen Verbesserung der globalen Supply-Chain-Leistung
Das Supply Chain Management nimmt dabei eine zentrale Rolle ein. * Stärkung und Weiterentwicklung einer robusten, zukunftssicheren und belastbaren Supply Chain, einschließlich Risikomanagement, Business Continuity und präventiver Stabilisierung kritischer Wertschöpfungsstufen * Einsatz moderner KPI- und Performance-Management-Methoden zur wirksamen Steuerung und kontinuierlichen Verbesserung der globalen Supply-Chain-Leistung
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IT Business Consultant Master Data Management (m/w/d)
IT Business Consultant Master Data Management (m/w/d)
Vetter Pharma-Fertigung GmbH & Co. KG
Ravensburg
• Betriebliches Gesundheitsmanagement (BGM) und verschiedene Fitness- und Sport-Angebote
• Betriebliches Gesundheitsmanagement (BGM) und verschiedene Fitness- und Sport-Angebote
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Begleitung externer und interner Studien in Zusammenarbeit mit dem Produktmanagement und externen Partnern aus dem dentalmedizinischen Umfeld * Schnittstelle zwischen Entwicklung, Regulatory, Marketing und Produktmanagement, um klinische Anforderungen in die Produktneuentwicklungen zu integrieren * Identifikation und Bewertung von Risiken im Zusammenhang mit KI-Algorithmen und Software-Funktionalitäten in enger Zusammenarbeit mit dem Risiko Management * Unterstützung im Bereich Usability, Post-Market Clinical Follow-up (PMCF) und Post-Market Surveillance (PMS) * Kooperationsfähigkeit, Kommunikationsstärke und Projektmanagementfähigkeiten
Begleitung externer und interner Studien in Zusammenarbeit mit dem Produktmanagement und externen Partnern aus dem dentalmedizinischen Umfeld * Schnittstelle zwischen Entwicklung, Regulatory, Marketing und Produktmanagement, um klinische Anforderungen in die Produktneuentwicklungen zu integrieren * Identifikation und Bewertung von Risiken im Zusammenhang mit KI-Algorithmen und Software-Funktionalitäten in enger Zusammenarbeit mit dem Risiko Management * Unterstützung im Bereich Usability, Post-Market Clinical Follow-up (PMCF) und Post-Market Surveillance (PMS) * Kooperationsfähigkeit, Kommunikationsstärke und Projektmanagementfähigkeiten
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Entwicklung und Implementierung von professionellen, effizienten und möglichst automatisierten und KI-gestützten Data-Management-Prozessen und Workflows - Wir suchen einen Data-Activation-Manager (m/w/d) * Tracking (Anforderungserhebung, Setup, Pixel-Integration und ‑Management) zur Sicherstellung der Datenqualität und -verfügbarkeit * Abstimmung mit dem Performance-Management zur effizienten und effektiven Nutzung der allokierten Media- und Marketingbudgets * Mehrjährige Data- und/oder Business-Analytics-Erfahrung im FMCG- oder OTC-Bereich auf Hersteller- und/oder Händlerseite * Fundierte, umfassende praktische Erfahrung in der Nutzung von Data-Analytics-Tools (GA4, Adobe etc.), ETL-Prozessen / -Tools und Datenvisualisierungs-Lösungen (bspw. Power BI
Entwicklung und Implementierung von professionellen, effizienten und möglichst automatisierten und KI-gestützten Data-Management-Prozessen und Workflows - Wir suchen einen Data-Activation-Manager (m/w/d) * Tracking (Anforderungserhebung, Setup, Pixel-Integration und ‑Management) zur Sicherstellung der Datenqualität und -verfügbarkeit * Abstimmung mit dem Performance-Management zur effizienten und effektiven Nutzung der allokierten Media- und Marketingbudgets * Mehrjährige Data- und/oder Business-Analytics-Erfahrung im FMCG- oder OTC-Bereich auf Hersteller- und/oder Händlerseite * Fundierte, umfassende praktische Erfahrung in der Nutzung von Data-Analytics-Tools (GA4, Adobe etc.), ETL-Prozessen / -Tools und Datenvisualisierungs-Lösungen (bspw. Power BI
Beliebte Jobs
- Study Nurse
- Medizinischer Dienst
- Klinikmanager
- Medizinische Verwaltung
- Medical Science Liaison
- Medizinische Informatik
- Legal Tech
- Clinical Research Associate
- Data Scientist
- Drug Safety Manager
- Medical advisor
- Clinical Affairs Manager
- Medical Affairs
- Clinical Data Manager
- Case Management
- Clinical Data Associate
Standorte
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