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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 sample metadata, and analysis outputs.
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 sample metadata, and analysis outputs.
The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * 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, * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use * Collaborate with Regulatory, Quality, and Clinical Affairs to ensure traceability and compliance of all diagnostic-related datasets - 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.
The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * 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, * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use * Collaborate with Regulatory, Quality, and Clinical Affairs to ensure traceability and compliance of all diagnostic-related datasets - 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.
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We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. For one of our sponsors we are looking for a Clinical Trial Manager to join the team. This role is part of the Clinical Study Unit and is accountable for the - strategic planning & management and performance of their assigned clinical trials from country allocation within feasibility process until study closure inclusive archiving. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. * Reviews the study scope of work, budget and protocol content and ensures the clinical (CRAs/Central Monitors) is aware of the ...
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. For one of our sponsors we are looking for a Clinical Trial Manager to join the team. This role is part of the Clinical Study Unit and is accountable for the - strategic planning & management and performance of their assigned clinical trials from country allocation within feasibility process until study closure inclusive archiving. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. * Reviews the study scope of work, budget and protocol content and ensures the clinical (CRAs/Central Monitors) is aware of the ...
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Product Manager VERTANICAL - Fokus Produktlaunch *
Product Manager VERTANICAL - Fokus Produktlaunch *
VERTANICAL
Gräfelfing bei München
Teilweise Home-Office
Du arbeitest eng mit unseren Fachabteilungen im Bereich Quality Assurance, Operations/Supply Chain, Scientific Marketing, Clinical Trials, Grafik und Web Development zusammen.
Du arbeitest eng mit unseren Fachabteilungen im Bereich Quality Assurance, Operations/Supply Chain, Scientific Marketing, Clinical Trials, Grafik und Web Development zusammen.
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Clinical Research Associate / Senior Clinical Research Associate
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO Deutschland GmbH
Munich
Teilweise Home-Office
Schnelle Bewerbung
As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
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 maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the ...
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 maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the ...
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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.
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
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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Regional Account Manager, Neurofibromatosis Region Ost (Rostock, Schwerin, Berlin, Leipzig, Dresden)
Regional Account Manager, Neurofibromatosis Region Ost (Rostock, Schwerin, Berlin, Leipzig, Dresden)
Alexion Pharma Germany GmbH
Germany - Munich
Or qualified nurse or other degree-level ancillary medical staff (e.g. Physiotherapy or Clinical Research Scientist) and/or equivalent experience. * Strong business, analytical and clinical acumen
Or qualified nurse or other degree-level ancillary medical staff (e.g. Physiotherapy or Clinical Research Scientist) and/or equivalent experience. * Strong business, analytical and clinical acumen
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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; * 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; * Balance usability, clarity, and aesthetics with clinical, technical, and regulatory constraints;
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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
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.
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;
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. 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.
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. 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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Schnelle Bewerbung
Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply.
Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply.
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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.
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
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
16 passende Jobs liegen außerhalb deiner Region
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Clinical Affairs Specialist (m/w/d)
Clinical Affairs Specialist (m/w/d)
corpuls - GS Elektromedizinische Geräte G. Stemple
Kaufering
Teilweise Home-Office
Anschreiben nicht erforderlich
Schnelle Bewerbung
Berufserfahrung in den relevanten Aufgabenbereichen von Clinical/Medical Affairs.
Berufserfahrung in den relevanten Aufgabenbereichen von Clinical/Medical Affairs.
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Schnelle Bewerbung
Sentec AG * Süddeutschland * 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 * Süddeutschland * 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
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Clinical Research Associate / Junior Monitor klinische Studien (m/w/d)
Clinical Research Associate / Junior Monitor klinische Studien (m/w/d)
wu personal GmbH
bundesweit, Home-Office
Teilweise Home-Office
Für unseren Auftraggeber, ein führendes, globales Unternehmen in der Medizintechnologie-Branche, suchen wir mehrere Mitarbeiter als Clinical Research Associate / Junior Monitor (m/w/d) für das Monitoring klinischer Studien. * Durchführung von Monitoring-Aktivitäten gemäß Prüfplan bzw. Monitoring-Plan, Standardarbeitsanweisungen guter klinischer Praxis (Good Clinical Practice) und regulatorischen Vorgaben * Nachweisbare Berufserfahrung im klinischen Monitoring (Clinical Research Monitoring), idealerweise 1 bis 3 Jahre
Für unseren Auftraggeber, ein führendes, globales Unternehmen in der Medizintechnologie-Branche, suchen wir mehrere Mitarbeiter als Clinical Research Associate / Junior Monitor (m/w/d) für das Monitoring klinischer Studien. * Durchführung von Monitoring-Aktivitäten gemäß Prüfplan bzw. Monitoring-Plan, Standardarbeitsanweisungen guter klinischer Praxis (Good Clinical Practice) und regulatorischen Vorgaben * Nachweisbare Berufserfahrung im klinischen Monitoring (Clinical Research Monitoring), idealerweise 1 bis 3 Jahre
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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
Clinical Affairs Specialist (m/w/d)
Clinical Affairs Specialist (m/w/d)
corpuls - GS Elektromedizinische Geräte G. Stemple
Kaufering
Teilweise Home-Office
Anschreiben nicht erforderlich
Berufserfahrung in den relevanten Aufgabenbereichen von Clinical/Medical Affairs
Berufserfahrung in den relevanten Aufgabenbereichen von Clinical/Medical Affairs