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- Garching bei München
- Gilching
- Fürstenfeldbruck
- Unterschleißheim
- Ottobrunn
- Aschheim
- Holzkirchen
- Planegg
- Eching
- Unterhaching
- Oberhaching
- Grasbrunn
- Neubiberg
- Oberschleißheim
- Grafing bei München
- Höhenkirchen-Siegertsbrunn
- Valley
- Otterfing
- Europa
- Westliches Europa
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164 Treffer für Clinical Research Jobs in Ottobrunn im Umkreis von 30 km
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At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate is a highly organized and dependable data professional with experience managing scientific or biomedical datasets, strong attention to detail, and the ability to coordinate effectively across diverse in a dynamic research environment. * Coordinate with wet laboratories, contract research organizations (CROs), and external collaborators to facilitate the transfer of imaging data and associated metadata. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or ...
At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate is a highly organized and dependable data professional with experience managing scientific or biomedical datasets, strong attention to detail, and the ability to coordinate effectively across diverse in a dynamic research environment. * Coordinate with wet laboratories, contract research organizations (CROs), and external collaborators to facilitate the transfer of imaging data and associated metadata. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or ...
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TUM Klinikum Rechts der Isar * München * Befristeter Vertrag * Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Ihr Universitätsklinikum im Herzen Münchens - Wir sind das TUM Klinikum Rechts der Isar und verlässlicher Arbeitgeber für rund 6.600 Mitarbeiter*innen. Als Uniklinikum widmen wir uns neben der Krankenversorgung auch der Forschung und Lehre – entsprechend unserem Leitbild „Wissenschaft Heilung“ und genießen national wie international einen ausgezeichneten Ruf. 160 unterschiedliche Berufsgruppen arbeiten Hand in Hand, um unseren Patient*innen eine optimale Behandlung zukommen zu lassen. Voll- und Teilzeit | befristet (12 Monate) * Sie übernehmen die Koordination und die Begleitung von Vertragsverhandlungen in enger Zusammenarbeit mit dem ECTU-Team, unseren Prüfärzt*innen sowie externen Partnern und Sponsoren
TUM Klinikum Rechts der Isar * München * Befristeter Vertrag * Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Ihr Universitätsklinikum im Herzen Münchens - Wir sind das TUM Klinikum Rechts der Isar und verlässlicher Arbeitgeber für rund 6.600 Mitarbeiter*innen. Als Uniklinikum widmen wir uns neben der Krankenversorgung auch der Forschung und Lehre – entsprechend unserem Leitbild „Wissenschaft Heilung“ und genießen national wie international einen ausgezeichneten Ruf. 160 unterschiedliche Berufsgruppen arbeiten Hand in Hand, um unseren Patient*innen eine optimale Behandlung zukommen zu lassen. Voll- und Teilzeit | befristet (12 Monate) * Sie übernehmen die Koordination und die Begleitung von Vertragsverhandlungen in enger Zusammenarbeit mit dem ECTU-Team, unseren Prüfärzt*innen sowie externen Partnern und Sponsoren
At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate is a highly organized and dependable data professional with experience managing scientific or biomedical datasets, strong attention to detail, and the ability to coordinate effectively across diverse in a dynamic research environment. * Coordinate with wet laboratories, contract research organizations (CROs), and external collaborators to facilitate the transfer of imaging data and associated metadata. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or ...
At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate is a highly organized and dependable data professional with experience managing scientific or biomedical datasets, strong attention to detail, and the ability to coordinate effectively across diverse in a dynamic research environment. * Coordinate with wet laboratories, contract research organizations (CROs), and external collaborators to facilitate the transfer of imaging data and associated metadata. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or ...
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Chemikant / Biologe / Mediziner / Gesundheitswissenschaftler / Pharmazeut / MTA als Medical Approver (m/w/d)
Chemikant / Biologe / Mediziner / Gesundheitswissenschaftler / Pharmazeut / MTA als Medical Approver (m/w/d)
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG
Garmisch-Partenkirchen, Bad Homburg, München
Teilweise Home-Office
Schnelle Bewerbung
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG * Garmisch-Partenkirchen, Bad Homburg, München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Als Spezialisten im Healthcare Markt führen wir jährlich über 2.000 Veranstaltungen durch. Unser Portfolio deckt dabei sämtliche Bereiche aus Kreation, Administration und Vor-Ort-Organisation ab: Ideenfindung und Konzeption, Auswahl von Location und Referierenden, Management der Teilnehmenden, Nachhaltigkeitsberatung, CME-Zertifizierung, Einhaltung der Pharma-Compliance-Regeln, technische Ausstattung, Catering und vieles mehr. Starte jetzt bei uns durch. Wir geben dir die Möglichkeit, dich mit deinen Talenten in einem abwechslungsreichen Beruf mit Perspektive auszuleben – als Teil eines jungen, engagierten Teams.
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG * Garmisch-Partenkirchen, Bad Homburg, München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Als Spezialisten im Healthcare Markt führen wir jährlich über 2.000 Veranstaltungen durch. Unser Portfolio deckt dabei sämtliche Bereiche aus Kreation, Administration und Vor-Ort-Organisation ab: Ideenfindung und Konzeption, Auswahl von Location und Referierenden, Management der Teilnehmenden, Nachhaltigkeitsberatung, CME-Zertifizierung, Einhaltung der Pharma-Compliance-Regeln, technische Ausstattung, Catering und vieles mehr. Starte jetzt bei uns durch. Wir geben dir die Möglichkeit, dich mit deinen Talenten in einem abwechslungsreichen Beruf mit Perspektive auszuleben – als Teil eines jungen, engagierten Teams.
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Mindestens 3 Jahre Erfahrung im Bereich klinische Studien / Clinical Research, idealerweise in der Medizintechnik, insbesondere in der Planung, Kooperation und operativen Durchführung klinischer Studien
Mindestens 3 Jahre Erfahrung im Bereich klinische Studien / Clinical Research, idealerweise in der Medizintechnik, insbesondere in der Planung, Kooperation und operativen Durchführung klinischer Studien
SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. * Demonstrated ability to apply problem solving techniques to resolve complex issues, and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity.
SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. * Demonstrated ability to apply problem solving techniques to resolve complex issues, and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity.
Define, implement and monitor end-to-end CP delivery workflows translating research, clinical, and diagnostic needs into practical execution, in collaboration with Quality Management and cross-functional teams, In this role, you will be instrumental in building the operational and data delivery foundation that connects computational pathology research with clinical and diagnostic impact. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use
Define, implement and monitor end-to-end CP delivery workflows translating research, clinical, and diagnostic needs into practical execution, in collaboration with Quality Management and cross-functional teams, In this role, you will be instrumental in building the operational and data delivery foundation that connects computational pathology research with clinical and diagnostic impact. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use
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Schnelle Bewerbung
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Ability to consult with , interpret research requirements, and determine statistical analysis strategies
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Ability to consult with , interpret research requirements, and determine statistical analysis strategies
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. * Prior experience working in clinical research 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. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training ...
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. * Prior experience working in clinical research 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. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training ...
Schnelle Bewerbung
Responsibility for the implementation of new medical practices, the evaluation of new indications, analysis of the status quo of current treatment and patient pathways, identification of patients for clinical research, and the development of a deep understanding of the respective indication area. * Development and implementation of the local medical strategy to support clinical practice and the objectives of the overall company.
Responsibility for the implementation of new medical practices, the evaluation of new indications, analysis of the status quo of current treatment and patient pathways, identification of patients for clinical research, and the development of a deep understanding of the respective indication area. * Development and implementation of the local medical strategy to support clinical practice and the objectives of the overall company.
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Schnelle Bewerbung
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
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Associate Director Country Operations Management
Associate Director Country Operations Management
Alexion Pharma Germany GmbH
Germany - Munich
Teilweise Home-Office
Schnelle Bewerbung
Contribute to Country feasibility analysis for new potential clinical trials (as applicable, depending on the direct reports the LM will be managing). Maintain tools to document and track clinical monitoring activities as required.
Contribute to Country feasibility analysis for new potential clinical trials (as applicable, depending on the direct reports the LM will be managing). Maintain tools to document and track clinical monitoring activities as required.
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Site Activation Manager (Contract Specialist - Germany - hybrid in München)
Site Activation Manager (Contract Specialist - Germany - hybrid in München)
Syneos Health Inc.
München
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. For one of our sponsors we are currently recruiting for a contract specialist / financial clinical operations specialist to join the team. * Excellent understanding of clinical trial process across Phases II-IV and ICH GCP * Good understanding clinical protocols and associated study specifications.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. For one of our sponsors we are currently recruiting for a contract specialist / financial clinical operations specialist to join the team. * Excellent understanding of clinical trial process across Phases II-IV and ICH GCP * Good understanding clinical protocols and associated study specifications.
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Director Medical Affairs Medical Lead HIV (m/f/d)
Director Medical Affairs Medical Lead HIV (m/f/d)
Healthcare Society e.V.
Munich Prinzregentenplatz
Teilweise Home-Office
Beyond our medicines, we are proud of our deep connection with the HIV community and work with to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response. You will work closely with various cross-functional counterparts and teams in commercial (across brands), market access, clinical operations etc. to ensure a well-balanced portfolio approach to ViiV's national promotional and scientific meetings and materials, pricing and reimbursement operations as well as clinical studies.
Beyond our medicines, we are proud of our deep connection with the HIV community and work with to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response. You will work closely with various cross-functional counterparts and teams in commercial (across brands), market access, clinical operations etc. to ensure a well-balanced portfolio approach to ViiV's national promotional and scientific meetings and materials, pricing and reimbursement operations as well as clinical studies.
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
Noch nichts dabei? Es gibt 149 weitere Jobs, die zu deiner Suche passen könnten
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Schnelle Bewerbung
This role requires strong product thinking, hands-on design execution, and close collaboration with Product Management, Engineering, and clinical stakeholders. You will directly contribute to Custom Surgical's growth by improving usability, reducing friction in clinical workflows, and helping shape future AI-enabled product experiences. * Translate clinical and operational workflows into intuitive user journeys and interfaces; * Conduct and synthesize user research, usability testing, and feedback from clinicians and internal teams; * Balance usability, clarity, and aesthetics with clinical, technical, and regulatory constraints;
This role requires strong product thinking, hands-on design execution, and close collaboration with Product Management, Engineering, and clinical stakeholders. You will directly contribute to Custom Surgical's growth by improving usability, reducing friction in clinical workflows, and helping shape future AI-enabled product experiences. * Translate clinical and operational workflows into intuitive user journeys and interfaces; * Conduct and synthesize user research, usability testing, and feedback from clinicians and internal teams; * Balance usability, clarity, and aesthetics with clinical, technical, and regulatory constraints;
NEU
Schnelle Bewerbung
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
NEU
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
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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.
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.
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Junior Datenanalyst Operations Research (m/w/d)
Junior Datenanalyst Operations Research (m/w/d)
IABG Industrieanlagen - Betriebsgesellschaft mbH
Ottobrunn bei München, Hamburg
Teilweise Home-Office
Möchten Sie nach einer strukturierten Einarbeitung an der Analyse von Fähigkeiten der Bundeswehr und anderer europäischer Streitkräfte unter Anwendung von Operations-Research-Methoden und quantitativer Datenanalyse mitwirken? Analyse von Fähigkeiten der Bundeswehr sowie anderer europäischer Streitkräfte unter Anwendung von Methoden des Operations Research (OR) und quantitativer Datenanalyse nach gründlicher Einarbeitung - Abgeschlossenes Studium im Bereich Mathematik, Soziologie, Psychologie, Wirtschaftswissenschaften, vorzugsweise mit der Vertiefungsrichtung Operations Research, oder vergleichbar
Möchten Sie nach einer strukturierten Einarbeitung an der Analyse von Fähigkeiten der Bundeswehr und anderer europäischer Streitkräfte unter Anwendung von Operations-Research-Methoden und quantitativer Datenanalyse mitwirken? Analyse von Fähigkeiten der Bundeswehr sowie anderer europäischer Streitkräfte unter Anwendung von Methoden des Operations Research (OR) und quantitativer Datenanalyse nach gründlicher Einarbeitung - Abgeschlossenes Studium im Bereich Mathematik, Soziologie, Psychologie, Wirtschaftswissenschaften, vorzugsweise mit der Vertiefungsrichtung Operations Research, oder vergleichbar
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→ Erfahrung in Recruiting, Personalauswahl, Talent Research oder Projektkoordination
→ Erfahrung in Recruiting, Personalauswahl, Talent Research oder Projektkoordination
NEU
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Research Services Manager (w/m/d)
Research Services Manager (w/m/d)
Hogan Lovells International LLP
Düsseldorf, Frankfurt am Main, München
Zur Verstärkung unseres Knowledge-Teams suchen wir Sie an einem unserer Standorte als Research Services Manager (w/m/d) Als Research Services Manager (w/m/d) leiten Sie das Team an mehreren deutschen Standorten, stellen die qualitativ hochwertige Versorgung unserer Anwält*innen und Fachkräfte mit rechtlichen, wirtschaftlichen und strategischen Informationen sicher und gestalten aktiv die Weiterentwicklung unseres globalen Research-Services-Netzwerks mit. * Operative Leitung des Research Services Teams mit 5 Mitarbeitenden an vier deutschen Standorten, einschließlich Mitarbeiterentwicklung und Recruiting * Sicherstellung und Weiterentwicklung des qualitativ hochwertigen Research Serviceangebots * Beitrag zur globalen Research-Services-Strategie und enge Zusammenarbeit mit internationalen Kolleg*innen bei der Evaluierung und Weiterentwicklung von Ressourcen und Serviceangeboten
Zur Verstärkung unseres Knowledge-Teams suchen wir Sie an einem unserer Standorte als Research Services Manager (w/m/d) Als Research Services Manager (w/m/d) leiten Sie das Team an mehreren deutschen Standorten, stellen die qualitativ hochwertige Versorgung unserer Anwält*innen und Fachkräfte mit rechtlichen, wirtschaftlichen und strategischen Informationen sicher und gestalten aktiv die Weiterentwicklung unseres globalen Research-Services-Netzwerks mit. * Operative Leitung des Research Services Teams mit 5 Mitarbeitenden an vier deutschen Standorten, einschließlich Mitarbeiterentwicklung und Recruiting * Sicherstellung und Weiterentwicklung des qualitativ hochwertigen Research Serviceangebots * Beitrag zur globalen Research-Services-Strategie und enge Zusammenarbeit mit internationalen Kolleg*innen bei der Evaluierung und Weiterentwicklung von Ressourcen und Serviceangeboten
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Secure Research Data Storage Engineer (m/w/d)
Secure Research Data Storage Engineer (m/w/d)
Leibniz-Rechenzentrum (LRZ) der Bayerischen Akademie der Wissenschaften
Garching bei München
Teilweise Home-Office
Schnelle Bewerbung
Mit deiner Arbeit unterstützt Du Forschungsverbünde wie das Deutsche Humangenom-Phenomarchiv (GHGA) oder die Bavarian Cloud for Health Research (BCHR) und leistest damit einen zentralen Beitrag zur professionellen und vertrauenswürdigen Nutzung sensibler Forschungsdaten – ein wichtiger Baustein für die Spitzenforschung in Deutschland und Europa.
Mit deiner Arbeit unterstützt Du Forschungsverbünde wie das Deutsche Humangenom-Phenomarchiv (GHGA) oder die Bavarian Cloud for Health Research (BCHR) und leistest damit einen zentralen Beitrag zur professionellen und vertrauenswürdigen Nutzung sensibler Forschungsdaten – ein wichtiger Baustein für die Spitzenforschung in Deutschland und Europa.
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Referent Finance & Research - Kapitalanlage Real Estate (d/w/m)
Referent Finance & Research - Kapitalanlage Real Estate (d/w/m)
Versicherungskammer Real Estate GmbH
München
Teilweise Home-Office
Schnelle Bewerbung
Du wirkst aktiv an der Erweiterung und Optimierung unseres Marktscreenings sowie Researchs mit und arbeitest dabei eng mit dem Investment Management zusammen. Weitere praktische Erfahrung im Finanz- oder Rechnungswesen sowie Research, vorzugsweise zusätzlich gesammelt während des Studiums sind ein Plus. * Ein ausgeprägtes crossfunktionales Mindset und die Fähigkeit, wissenschaftliche Erkenntnisse in praxisrelevante Research-Anforderungen und Analysen zu übertragen.
Du wirkst aktiv an der Erweiterung und Optimierung unseres Marktscreenings sowie Researchs mit und arbeitest dabei eng mit dem Investment Management zusammen. Weitere praktische Erfahrung im Finanz- oder Rechnungswesen sowie Research, vorzugsweise zusätzlich gesammelt während des Studiums sind ein Plus. * Ein ausgeprägtes crossfunktionales Mindset und die Fähigkeit, wissenschaftliche Erkenntnisse in praxisrelevante Research-Anforderungen und Analysen zu übertragen.
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Lead Research Engineer (f/m/d): Foundation and World Models on Structured Data
Lead Research Engineer (f/m/d): Foundation and World Models on Structured Data
SAP SE
Garching bei München, DE, 85748
At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and models, with the goal to publish benchmarks and models at scientific conferences and in the open-source community. Define and drive open source model and software contributions based on research deliverables. Knowledge of latest research and development trends in Foundation Models on Structured Data.
At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and models, with the goal to publish benchmarks and models at scientific conferences and in the open-source community. Define and drive open source model and software contributions based on research deliverables. Knowledge of latest research and development trends in Foundation Models on Structured Data.
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Standorte
- München
- Starnberg
- Garching bei München
- Gilching
- Fürstenfeldbruck
- Unterschleißheim
- Ottobrunn
- Aschheim
- Holzkirchen
- Planegg
- Eching
- Unterhaching
- Oberhaching
- Grasbrunn
- Neubiberg
- Oberschleißheim
- Grafing bei München
- Höhenkirchen-Siegertsbrunn
- Valley
- Otterfing
- Europa
- Westliches Europa
- Süddeutschland
- Bayern
- Neckarland-Schwaben
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- Oberbayern