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Schnelle Bewerbung
Sentec AG * München * Feste Anstellung * Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Sentec ist ein schweizerisch-amerikanisches Medizintechnikunternehmen, das sich auf die Beatmungsmedizin spezialisiert. Seit seiner Gründung im Jahr 1999 verfolgt Sentec einen Deep-Tech-Ansatz, der auf fortschrittlicher Wissenschaft und avantgardistischen Technologien basiert, um Patienten mit Atemwegserkrankungen in allen Pflegebereichen zu versorgen. Sentec bietet medizinischen Fachkräften auf der ganzen Welt nicht-invasive, kontinuierliche Überwachung und effektive therapeutische Lösungen. Sentec erhielt die Auszeichnung ‚Top Company' von Kununu in den Jahren 2025 und 2026. Ihre Aufgaben * Demonstration, Schulung und Einweisung in das Sentec-Portfolio bei klinischen Anwendern vor Ort * Troubleshooting und First-Level-Support für bestehende Kunden
Sentec AG * München * Feste Anstellung * Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Sentec ist ein schweizerisch-amerikanisches Medizintechnikunternehmen, das sich auf die Beatmungsmedizin spezialisiert. Seit seiner Gründung im Jahr 1999 verfolgt Sentec einen Deep-Tech-Ansatz, der auf fortschrittlicher Wissenschaft und avantgardistischen Technologien basiert, um Patienten mit Atemwegserkrankungen in allen Pflegebereichen zu versorgen. Sentec bietet medizinischen Fachkräften auf der ganzen Welt nicht-invasive, kontinuierliche Überwachung und effektive therapeutische Lösungen. Sentec erhielt die Auszeichnung ‚Top Company' von Kununu in den Jahren 2025 und 2026. Ihre Aufgaben * Demonstration, Schulung und Einweisung in das Sentec-Portfolio bei klinischen Anwendern vor Ort * Troubleshooting und First-Level-Support für bestehende Kunden
Arthrex GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Wir gehören zu den weltweit führenden Unternehmen im Bereich Orthopädie, Arthroskopie, Sportmedizin und Orthobiologie. Getreu unserer Mission Helping Surgeons Treat Their Patients Better entwickeln wir seit 40 Jahren innovative Produkte und Operationsverfahren. Arthrex wurde 1981 in München gegründet - heute befindet sich unser Hauptsitz in Naples (Florida, USA) mit weiteren Niederlassungen in 29 Ländern. Unsere Firmenkultur ist geprägt von einer länderübergreifenden Zusammenarbeit sowie einem Austausch mit Kolleginnen und Kollegen unterschiedlicher Nationalitäten. Die Erschließung neuer Geschäftsfelder und die Erweiterung unserer Produktpalette tragen zu einem stetigen Wachstum bei und lassen uns auch in Zukunft federführend bei der Entwicklung qualitativ hochwertiger ...
Arthrex GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Wir gehören zu den weltweit führenden Unternehmen im Bereich Orthopädie, Arthroskopie, Sportmedizin und Orthobiologie. Getreu unserer Mission Helping Surgeons Treat Their Patients Better entwickeln wir seit 40 Jahren innovative Produkte und Operationsverfahren. Arthrex wurde 1981 in München gegründet - heute befindet sich unser Hauptsitz in Naples (Florida, USA) mit weiteren Niederlassungen in 29 Ländern. Unsere Firmenkultur ist geprägt von einer länderübergreifenden Zusammenarbeit sowie einem Austausch mit Kolleginnen und Kollegen unterschiedlicher Nationalitäten. Die Erschließung neuer Geschäftsfelder und die Erweiterung unserer Produktpalette tragen zu einem stetigen Wachstum bei und lassen uns auch in Zukunft federführend bei der Entwicklung qualitativ hochwertiger ...
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Clinical Specialist Sports - Medicine & Arthroplasty (m/w/d)
Clinical Specialist Sports - Medicine & Arthroplasty (m/w/d)
Arthrex GmbH
München
Teilweise Home-Office
Arthrex GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Wir gehören zu den weltweit führenden Unternehmen im Bereich Orthopädie, Arthroskopie, Sportmedizin und Orthobiologie. Getreu unserer Mission Helping Surgeons Treat Their Patients Better entwickeln wir seit 40 Jahren innovative Produkte und Operationsverfahren. Arthrex wurde 1981 in München gegründet - heute befindet sich unser Hauptsitz in Naples (Florida, USA) mit weiteren Niederlassungen in 29 Ländern. Unsere Firmenkultur ist geprägt von einer länderübergreifenden Zusammenarbeit sowie einem Austausch mit Kolleginnen und Kollegen unterschiedlicher Nationalitäten. Die Erschließung neuer Geschäftsfelder und die Erweiterung unserer Produktpalette tragen zu einem stetigen Wachstum bei und lassen uns auch in Zukunft federführend bei der Entwicklung qualitativ hochwertiger ...
Arthrex GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Wir gehören zu den weltweit führenden Unternehmen im Bereich Orthopädie, Arthroskopie, Sportmedizin und Orthobiologie. Getreu unserer Mission Helping Surgeons Treat Their Patients Better entwickeln wir seit 40 Jahren innovative Produkte und Operationsverfahren. Arthrex wurde 1981 in München gegründet - heute befindet sich unser Hauptsitz in Naples (Florida, USA) mit weiteren Niederlassungen in 29 Ländern. Unsere Firmenkultur ist geprägt von einer länderübergreifenden Zusammenarbeit sowie einem Austausch mit Kolleginnen und Kollegen unterschiedlicher Nationalitäten. Die Erschließung neuer Geschäftsfelder und die Erweiterung unserer Produktpalette tragen zu einem stetigen Wachstum bei und lassen uns auch in Zukunft federführend bei der Entwicklung qualitativ hochwertiger ...
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Schnelle Bewerbung
Our Clinical Graduate Program is designed to help early-career professionals contribute to solutions that transform patient lives. As a part of the Field Clinical Specialist team, you'll play a crucial role in partnering with clinical professionals to deliver our patient-focused therapies including proctoring, training and education. The Clinical Graduate Program starts in October 2026, offering a structured 12-month fixed-term contract. * Intensive Educational Academy: Dive into a 12-month program that enhances your product knowledge, cardiovascular expertise, clinical understanding and fundamental commercial skills. * Hands-On Experience: Work alongside certified Field Clinical Specialists (FCS) to support case coverage, troubleshoot issues, program devices and follow up with patients on our cutting-edge product range.
Our Clinical Graduate Program is designed to help early-career professionals contribute to solutions that transform patient lives. As a part of the Field Clinical Specialist team, you'll play a crucial role in partnering with clinical professionals to deliver our patient-focused therapies including proctoring, training and education. The Clinical Graduate Program starts in October 2026, offering a structured 12-month fixed-term contract. * Intensive Educational Academy: Dive into a 12-month program that enhances your product knowledge, cardiovascular expertise, clinical understanding and fundamental commercial skills. * Hands-On Experience: Work alongside certified Field Clinical Specialists (FCS) to support case coverage, troubleshoot issues, program devices and follow up with patients on our cutting-edge product range.
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Associate Director Regulatory Affairs – CMC Lead*
Associate Director Regulatory Affairs – CMC Lead*
Immatics Biotechnologies GmbH
Tübingen, München, Home-Office
Teilweise Home-Office
In this role, you will provide strategic CMC regulatory leadership for innovative oncology biopharmaceutical and ATMP programs across clinical development phases. You will independently lead EU CMC regulatory strategy and execution for assigned programs across early and late-stage clinical development. * Own EU CMC regulatory strategy for assigned clinical-stage programs (phase I–III). * Lead preparation and coordination of CMC/ GMP documentation for submission of initial clinical trial applications as well as Substantial Modifications. * Strong experience preparing CMC-related information/ documents for clinical trial applications and supporting Health Authority interactions.
In this role, you will provide strategic CMC regulatory leadership for innovative oncology biopharmaceutical and ATMP programs across clinical development phases. You will independently lead EU CMC regulatory strategy and execution for assigned programs across early and late-stage clinical development. * Own EU CMC regulatory strategy for assigned clinical-stage programs (phase I–III). * Lead preparation and coordination of CMC/ GMP documentation for submission of initial clinical trial applications as well as Substantial Modifications. * Strong experience preparing CMC-related information/ documents for clinical trial applications and supporting Health Authority interactions.
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Enge Zusammenarbeit mit Germany, Marketing, Produktmanagement und Clinical Services
Enge Zusammenarbeit mit Germany, Marketing, Produktmanagement und Clinical Services
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Consultant / Senior Consultant Health Care Technology (m/w/d)
Consultant / Senior Consultant Health Care Technology (m/w/d)
Deloitte
Berlin, Düsseldorf, Frankfurt (Main), Köln, Hamburg, München, Stuttgart
Teilweise Home-Office
Anschreiben nicht erforderlich
Spezialisierte und fundierte Kenntnisse in Interoperabilitätsstandards (z. B. HL7 v2, HL7 FHIR, IHE, DICOM), KI und Clinical Decision Support (CDSS) und der Konzeption von Systemarchitekturen, Schnittstellenkonzepten, Datenmodellen und Integrationsdesign im klinischen Umfeld
Spezialisierte und fundierte Kenntnisse in Interoperabilitätsstandards (z. B. HL7 v2, HL7 FHIR, IHE, DICOM), KI und Clinical Decision Support (CDSS) und der Konzeption von Systemarchitekturen, Schnittstellenkonzepten, Datenmodellen und Integrationsdesign im klinischen Umfeld
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Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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Als Clinical Operations Specialist führen und koordinieren Sie Aktivitäten im Zusammenhang mit Einreichungen gemäß ICH GCP, internationalen und lokalen Vorschriften sowie relevanten GSK-Standards.
Als Clinical Operations Specialist führen und koordinieren Sie Aktivitäten im Zusammenhang mit Einreichungen gemäß ICH GCP, internationalen und lokalen Vorschriften sowie relevanten GSK-Standards.
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Schnelle Bewerbung
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
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
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany
NEU
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Schnelle Bewerbung
PSIMedical Monitorsprovide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
PSIMedical Monitorsprovide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
Schnelle Bewerbung
We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity. * Communicate study challenges to Clinical Data Science group and work out data-driven solutions * Clinical Study Lead/Manager experience * Knowledge of theprocessand functions in clinical trials, ability to understand the protocol and study associated risks
We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity. * Communicate study challenges to Clinical Data Science group and work out data-driven solutions * Clinical Study Lead/Manager experience * Knowledge of theprocessand functions in clinical trials, ability to understand the protocol and study associated risks
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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.
Schnelle Bewerbung
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 * 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 * 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
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Schnelle Bewerbung
Parts of our apps need to be rebuilt from scratch, the user experience has room to grow significantly, and we believe that great product work can push real-world outcomes well beyond what our clinical studies already proved.
Parts of our apps need to be rebuilt from scratch, the user experience has room to grow significantly, and we believe that great product work can push real-world outcomes well beyond what our clinical studies already proved.
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Schnelle Bewerbung
You will work on mobile software used daily in clinical environments, where reliability, performance, and efficiency are critical. 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. * Direct impact on products used in real clinical environments worldwide;
You will work on mobile software used daily in clinical environments, where reliability, performance, and efficiency are critical. 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. * Direct impact on products used in real clinical environments worldwide;
Schnelle Bewerbung
Reliability, performance, and scalability are critical, as these applications are used daily in real clinical environments. * Direct impact on mission-critical software used in clinical workflows worldwide;
Reliability, performance, and scalability are critical, as these applications are used daily in real clinical environments. * Direct impact on mission-critical software used in clinical workflows worldwide;
Schnelle Bewerbung
He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives.
He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives.
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Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards.
Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards.
Schnelle Bewerbung
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. * 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.
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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.
Schnelle Bewerbung
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany
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Schnelle Bewerbung
Myoncare collects clinical patient data thanks to audited blockchain, without its own access, and ensures its security through encryption.
Myoncare collects clinical patient data thanks to audited blockchain, without its own access, and ensures its security through encryption.
6 passende Jobs liegen außerhalb deiner Region
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Clinical Support Specialist / Anwendungsexperte (m/w/d)
Clinical Support Specialist / Anwendungsexperte (m/w/d)
ACANDIS GmbH
Norddeutschland, Ostdeutschland, Süddeutschland, Westdeutschland
Schnelle Bewerbung
Zum nächstmöglichen Zeitpunkt suchen wir einen Clinical Support Specialist / Anwendungsexperte (m/w/d) Als Clinical Support Specialist Deutschland arbeiten Sie an der Schnittstelle zwischen unseren Technologien und den Ärzten in den Kliniken. * Enger Austausch innerhalb des Clinical Support Teams sowie mit den Unternehmensbereichen Entwicklung, Klinische Forschung und Medical Affairs
Zum nächstmöglichen Zeitpunkt suchen wir einen Clinical Support Specialist / Anwendungsexperte (m/w/d) Als Clinical Support Specialist Deutschland arbeiten Sie an der Schnittstelle zwischen unseren Technologien und den Ärzten in den Kliniken. * Enger Austausch innerhalb des Clinical Support Teams sowie mit den Unternehmensbereichen Entwicklung, Klinische Forschung und Medical Affairs