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16.144 Treffer für Trial Management Jobs in Westdeutschland im Umkreis von 30 km
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Pharmacovigilance Manager (m/w/d) Manager/in für Arzneimittelsicherheit (m/w/d)
Pharmacovigilance Manager (m/w/d) Manager/in für Arzneimittelsicherheit (m/w/d)
Biofrontera AG
Leverkusen
Sie übernehmen die Verantwortung für den einwandfreien Informationsfluss aller beteiligten internen (z.B. Medical Affairs, Regulatory Affairs, Clinical Trial Management, Quality Management) und externen Partner zur Pharmakovigilanz * Sie unterstützen und reviewen die regelmäßige Berichterstattung und das Risikomanagement * Sie interessieren sich nicht nur für Pharmacovigilance, sondern auch Quality Management Themen * Sie unterstützen die QM-Abteilungen bei Quality-Prozessen wie z.B. Dokumentenlenkung, Abweichungen, Change-Management, Korrektur- und Vorbeugemaßnahmen sowie Schulungen und Dienstleisterqualifizierung
Sie übernehmen die Verantwortung für den einwandfreien Informationsfluss aller beteiligten internen (z.B. Medical Affairs, Regulatory Affairs, Clinical Trial Management, Quality Management) und externen Partner zur Pharmakovigilanz * Sie unterstützen und reviewen die regelmäßige Berichterstattung und das Risikomanagement * Sie interessieren sich nicht nur für Pharmacovigilance, sondern auch Quality Management Themen * Sie unterstützen die QM-Abteilungen bei Quality-Prozessen wie z.B. Dokumentenlenkung, Abweichungen, Change-Management, Korrektur- und Vorbeugemaßnahmen sowie Schulungen und Dienstleisterqualifizierung
Noch nichts dabei? Es gibt 16143 weitere Jobs, die zu deiner Suche passen könnten
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Senior Clinical Trial Physician (m|f|d)
Senior Clinical Trial Physician (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As a Senior Clinical Trial Physician, you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning, execution, and supervision of clinical trials in hemato-oncology. * You will lead the design and implementation of clinical trial protocols, ensuring adherence to ICH-GCP, ethical standards, and regulatory requirements. * You will provide medical supervision of ongoing trials, working closely with Clinical Operations and Medical Monitors, and support protocol
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As a Senior Clinical Trial Physician, you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning, execution, and supervision of clinical trials in hemato-oncology. * You will lead the design and implementation of clinical trial protocols, ensuring adherence to ICH-GCP, ethical standards, and regulatory requirements. * You will provide medical supervision of ongoing trials, working closely with Clinical Operations and Medical Monitors, and support protocol
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Erstellung aller erforderlichen Data-Management-Dokumente, einschließlich Data Management Plans (DMP), eCRFs, Annotations und Trial Validation Plans (TVP) * Überwachung der Datenqualität inklusive Query-Managements und Programmierung von Edit Checks (z. B. in SQL) * Sie haben ein abgeschlossenes Studium in Medizinischer Dokumentation, Medizinischer Informatik, Digital Health Management, Health Care Management oder einem naturwissenschaftlichen Studiengang mit entsprechender Weiterbildung. * Erfahrung im Umgang mit eCRF-Systemen sowie Kenntnisse in Datenvalidierung, Edit-Check- Erstellung, Query-Management und der Verarbeitung externer Datenquellen (Labore, ePRO/eCOA etc.)
Erstellung aller erforderlichen Data-Management-Dokumente, einschließlich Data Management Plans (DMP), eCRFs, Annotations und Trial Validation Plans (TVP) * Überwachung der Datenqualität inklusive Query-Managements und Programmierung von Edit Checks (z. B. in SQL) * Sie haben ein abgeschlossenes Studium in Medizinischer Dokumentation, Medizinischer Informatik, Digital Health Management, Health Care Management oder einem naturwissenschaftlichen Studiengang mit entsprechender Weiterbildung. * Erfahrung im Umgang mit eCRF-Systemen sowie Kenntnisse in Datenvalidierung, Edit-Check- Erstellung, Query-Management und der Verarbeitung externer Datenquellen (Labore, ePRO/eCOA etc.)
Global CAR-T Medical Manager (m|f|d)
Global CAR-T Medical Manager (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product , is currently undergoing pivotal clinical trials on a global scale. * Working with free and self-determined time management, also mobile working
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product , is currently undergoing pivotal clinical trials on a global scale. * Working with free and self-determined time management, also mobile working
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Technical Product Sales Manager - Food Processing & Packaging (m/f/d)
Technical Product Sales Manager - Food Processing & Packaging (m/f/d)
GEA Food Solutions Germany GmbH
Biedenkopf-Wallau
Act as the primary link between offices, customers, , and internal departments (Engineering, Marketing, Order Management, Application Engineers, Planning, Trial Centre) to ensure a smooth sales trajectory * Central management of key global accounts for slicing & packaging, maintaining high-level relationships and understanding their unique business needs
Act as the primary link between offices, customers, , and internal departments (Engineering, Marketing, Order Management, Application Engineers, Planning, Trial Centre) to ensure a smooth sales trajectory * Central management of key global accounts for slicing & packaging, maintaining high-level relationships and understanding their unique business needs
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Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). * Excellent organizational and time management abilities.
Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). * Excellent organizational and time management abilities.
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Associate Principal/Principal Medical Writers (F, M or D)
Associate Principal/Principal Medical Writers (F, M or D)
Trilogy Writing & Consulting GmbH
Frankfurt am Main
Work in the client's regulatory document management systems. - Must have experience as the lead writer with multiple-document projects with global, multinational teams, including team management, project management, review management, and budget oversight. - Must have in-depth working knowledge of the relevant regulatory guidance (e.g. ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance. - Competency in the use of document management systems and review tools.
Work in the client's regulatory document management systems. - Must have experience as the lead writer with multiple-document projects with global, multinational teams, including team management, project management, review management, and budget oversight. - Must have in-depth working knowledge of the relevant regulatory guidance (e.g. ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance. - Competency in the use of document management systems and review tools.
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As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental interests and is consistent with ICON's rules, procedures, and policies. * Works cross functionally with internal stakeholders in support of timely site start up and maintenance for the conduct of clinical trials including accurate forecast of contract execution timelines
As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental interests and is consistent with ICON's rules, procedures, and policies. * Works cross functionally with internal stakeholders in support of timely site start up and maintenance for the conduct of clinical trials including accurate forecast of contract execution timelines
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Recor Medical Ltd. / Recor Medical Europe GmbH, headquartered in Palo Alto, CA, is an innovative medical technology company focused on transforming the management of hypertension, the leading cardiovascular risk factor in the world. * Keep up to date on clinical trials, both investigator initiated and external studies, that can be used to improve clinical and health economic value messaging for Recor Medical products or categories * Self-motivated with excellent time management skills
Recor Medical Ltd. / Recor Medical Europe GmbH, headquartered in Palo Alto, CA, is an innovative medical technology company focused on transforming the management of hypertension, the leading cardiovascular risk factor in the world. * Keep up to date on clinical trials, both investigator initiated and external studies, that can be used to improve clinical and health economic value messaging for Recor Medical products or categories * Self-motivated with excellent time management skills
Senior Project Manager - Drug Development (m|f|d)
Senior Project Manager - Drug Development (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. In this role, you will lead the cross-functional project management effort, ensuring that timelines, interdependencies, and critical deliverables are aligned across all contributing functions. * Lead global project management activities for assigned drug-development programs, ensuring coordinated execution across key functions such as clinical, regulatory, CMC, safety, medical, biostatistics, and operations. * You have a proven track record of managing complex cross-functional projects in a matrix environment, with strong project planning, timeline management, and organizational skills. * You possess excellent written and verbal communication skills in English and are highly proficient i
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. In this role, you will lead the cross-functional project management effort, ensuring that timelines, interdependencies, and critical deliverables are aligned across all contributing functions. * Lead global project management activities for assigned drug-development programs, ensuring coordinated execution across key functions such as clinical, regulatory, CMC, safety, medical, biostatistics, and operations. * You have a proven track record of managing complex cross-functional projects in a matrix environment, with strong project planning, timeline management, and organizational skills. * You possess excellent written and verbal communication skills in English and are highly proficient i
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The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical Chemistry and Immunoassays. * Product Lifecycle: Forecasting, launches, obsolescence/discontinuation, technical support, ring trials, QC updates, complaint handling. * 5+ years in IVD product marketing/management.
The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical Chemistry and Immunoassays. * Product Lifecycle: Forecasting, launches, obsolescence/discontinuation, technical support, ring trials, QC updates, complaint handling. * 5+ years in IVD product marketing/management.
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * Your profile is rounded by a solid understanding of drug development and regulatory frameworks (ICH, EMA, FDA), excellent project management skills, and the ability to communicate complex scientific data clearly in English. * Working with free and self-determined time management, also mobile working
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * Your profile is rounded by a solid understanding of drug development and regulatory frameworks (ICH, EMA, FDA), excellent project management skills, and the ability to communicate complex scientific data clearly in English. * Working with free and self-determined time management, also mobile working
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * You lead / co-lead with GSC, the design and implementation of processes for GSC activities, IT tools (including respective CSV), and work aids for clinical trials and commercial processes. * Working with free and self-determined time management, also mobile working
We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * You lead / co-lead with GSC, the design and implementation of processes for GSC activities, IT tools (including respective CSV), and work aids for clinical trials and commercial processes. * Working with free and self-determined time management, also mobile working
Senior Clinical Scientist – Clinical Drug Development (m|f|d)
Senior Clinical Scientist – Clinical Drug Development (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * Additionally, the design, drafting, and review of clinical trial protocols, amendments, and study-related documents fall within your scope of responsibility. * You demonstrate comprehensive expertise across the clinical data lifecycle—working backwards from the desired final readouts to plan early for the necessary data, overseeing capture, coordinating cleaning and integrity checks, and obtaining study results in collaboration with biostatistics, programming, data management, and medical monitoring teams—ensuring outputs that are decision-ready for regulatory and clinical use. * Working with free and self-determined time management, also mobile working
Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. * Additionally, the design, drafting, and review of clinical trial protocols, amendments, and study-related documents fall within your scope of responsibility. * You demonstrate comprehensive expertise across the clinical data lifecycle—working backwards from the desired final readouts to plan early for the necessary data, overseeing capture, coordinating cleaning and integrity checks, and obtaining study results in collaboration with biostatistics, programming, data management, and medical monitoring teams—ensuring outputs that are decision-ready for regulatory and clinical use. * Working with free and self-determined time management, also mobile working
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Vertriebsmitarbeiter (m/w/d) für Telematik- und Flottenmanagementlösungen
Vertriebsmitarbeiter (m/w/d) für Telematik- und Flottenmanagementlösungen
Ctrack Deutschland GmbH
Bissendorf, Westdeutschland, Mitteldeutschland, Süddeutschland
Teilweise Home-Office
Mit technischem Verständnis, Beratungskompetenz und Begeisterung für innovative Telematik- und Flottenmanagementlösungen unterstützt du Unternehmen dabei, ihre Fahrzeugflotte und Assets effizienter, sicherer und nachhaltiger zu gestalten. Als führendes Unternehmen im Bereich Software-as-a-Service (SaaS) bieten wir digitale Fuhrparkmanagement- und Telematiklösungen für unsere Kunden aus verschiedenen Branchen.
Mit technischem Verständnis, Beratungskompetenz und Begeisterung für innovative Telematik- und Flottenmanagementlösungen unterstützt du Unternehmen dabei, ihre Fahrzeugflotte und Assets effizienter, sicherer und nachhaltiger zu gestalten. Als führendes Unternehmen im Bereich Software-as-a-Service (SaaS) bieten wir digitale Fuhrparkmanagement- und Telematiklösungen für unsere Kunden aus verschiedenen Branchen.
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Kaufmännischer Mitarbeiter mit Assistenztätigkeiten Bauprojektmanagement - Frankfurt/Mainz (m/w/d)
Kaufmännischer Mitarbeiter mit Assistenztätigkeiten Bauprojektmanagement - Frankfurt/Mainz (m/w/d)
Vonovia
Frankfurt
Vonovia * Frankfurt * Unterstützung der Abteilungsleitung im Tagesgeschäft, bei der Vor- und Nachbereitung von Meetings sowie in der internen und externen Kommunikation * Schnittstelle zwischen den Teams (bereichsübergreifend) und der Abteilungsleitung * Begleitung des Abteilungsaustauschs inklusive Protokollführung und Nachverfolgung von Aufgaben * Erstellung aussagekräftiger Reportings und Kennzahlenübersichten * Prüfung von Projektunterlagen, Terminplänen und Kosten * Zusammenstellung relevanter Informationen und Erarbeitung fundierter Entscheidungsvorlagen, Präsentationsunterlagen sowie Dokumentationen * Koordination bereichsübergreifender, übergeordneter Projekte und maßgebliche Beteiligung an deren erfolgreicher Umsetzung - Dein Profil * Abgeschlossene kaufmännische oder technische Ausbildung bzw. abgeschlossenes Studium
Vonovia * Frankfurt * Unterstützung der Abteilungsleitung im Tagesgeschäft, bei der Vor- und Nachbereitung von Meetings sowie in der internen und externen Kommunikation * Schnittstelle zwischen den Teams (bereichsübergreifend) und der Abteilungsleitung * Begleitung des Abteilungsaustauschs inklusive Protokollführung und Nachverfolgung von Aufgaben * Erstellung aussagekräftiger Reportings und Kennzahlenübersichten * Prüfung von Projektunterlagen, Terminplänen und Kosten * Zusammenstellung relevanter Informationen und Erarbeitung fundierter Entscheidungsvorlagen, Präsentationsunterlagen sowie Dokumentationen * Koordination bereichsübergreifender, übergeordneter Projekte und maßgebliche Beteiligung an deren erfolgreicher Umsetzung - Dein Profil * Abgeschlossene kaufmännische oder technische Ausbildung bzw. abgeschlossenes Studium
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Servicetechniker / Haustechniker (w/m/d) für Gebäudetechnik & Facility Management
Servicetechniker / Haustechniker (w/m/d) für Gebäudetechnik & Facility Management
Apleona GmbH
Monheim am Rhein
Erste Erfahrungen im technischen Gebäudemanagement / Facility Management von Vorteil
Erste Erfahrungen im technischen Gebäudemanagement / Facility Management von Vorteil
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Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Düsseldorf
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Duisburg
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Bonn
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Köln
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Münster
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Bielefeld
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Aachen
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
Duales Studium BWL - Spezialisierung Logistikmanagement (B.A.) am Campus oder virtuell
IU Internationale Hochschule
Mainz
Anschreiben nicht erforderlich
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
Dann ist das Duale Studium BWL - Spezialisierung Logistikmanagement genau Dein Ding.
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- Frankfurt am Main
- Köln
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- Dortmund
- Essen
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- Bonn
- Bielefeld
- Duisburg
- Bochum
- Kassel
- Aachen
- Wiesbaden
- Mainz
- Koblenz
- Mönchengladbach
- Darmstadt
- Wuppertal
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- Europa
- Westliches Europa
- Westdeutschland
- Nordrhein-Westfalen
- Rheinland
- Hessen
- Ruhrgebiet
- Niederrhein
- Rheinland-Pfalz
- Münsterland
- Ostwestfalen-Lippe
- Bergisches Land