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55.611 Treffer für Clinical Data Management Jobs
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Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Actual position's title: Clinical Data * Participating
Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Actual position's title: Clinical Data * Participating
Noch nichts dabei? Es gibt 55610 weitere Jobs, die zu deiner Suche passen könnten
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In Ihrer Rolle als Clinical Data Manager stellen Sie die korrekte, vollständige und regelkonforme Erhebung sowie Aufbereitung der Studiendaten für die statistische Auswertung in Phase-I- und Phase-II-Studien sicher. * 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. * Sie verfügen
In Ihrer Rolle als Clinical Data Manager stellen Sie die korrekte, vollständige und regelkonforme Erhebung sowie Aufbereitung der Studiendaten für die statistische Auswertung in Phase-I- und Phase-II-Studien sicher. * 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. * Sie verfügen
NEU
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Clinical Research Associate (CRA) (m/w/d) - Onkologie (im Außendienst)
Clinical Research Associate (CRA) (m/w/d) - Onkologie (im Außendienst)
AstraZeneca
Sachsen-Anhalt
Teilweise Home-Office
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung einen Clinical Research Associate (CRA) (m/w/d) - Onkologie (im Außendienst) * Sie begeistern sich für innovative Ansätze im Monitoring wie beispielsweise Risk Based Quality Management und Remote Monitoring und bringen die Bereitschaft mit, sich kontinuierlich weiterzuentwickeln und neue Methoden erfolgreich umzusetzen. * Idealerweise haben Sie Erfahrung in der Anwendung elektronischer Case Report Forms (Web Based Data Capture) und der Erstellung von Monitoring Reports.
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung einen Clinical Research Associate (CRA) (m/w/d) - Onkologie (im Außendienst) * Sie begeistern sich für innovative Ansätze im Monitoring wie beispielsweise Risk Based Quality Management und Remote Monitoring und bringen die Bereitschaft mit, sich kontinuierlich weiterzuentwickeln und neue Methoden erfolgreich umzusetzen. * Idealerweise haben Sie Erfahrung in der Anwendung elektronischer Case Report Forms (Web Based Data Capture) und der Erstellung von Monitoring Reports.
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
AstraZeneca
bundesweit
Teilweise Home-Office
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
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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
You will review and analyze clinical trial data, contributing to Clinical Study Reports (CSRs), MAA/BLA submissions, and other regulatory documentation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. 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
You will review and analyze clinical trial data, contributing to Clinical Study Reports (CSRs), MAA/BLA submissions, and other regulatory documentation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. 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
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Clinical Study Project Management: Take full responsibility for clinical trials in the role as sponsor and of non-interventional healthcare studies in fully outsourced model, steering scope, timelines and budget while safeguarding patient safety and data integrity. * Experience: Professional experience in clinical research project management (pharmaceutical industry or contract research organization) are an asset, but we are also open for structured and well-organized graduates. Department Clinical Research - The Clinical Research team is responsible for the implementation of all clinical research projects, from planning to reporting. Projects comprise clinical trials as well as all types of non-inter
Clinical Study Project Management: Take full responsibility for clinical trials in the role as sponsor and of non-interventional healthcare studies in fully outsourced model, steering scope, timelines and budget while safeguarding patient safety and data integrity. * Experience: Professional experience in clinical research project management (pharmaceutical industry or contract research organization) are an asset, but we are also open for structured and well-organized graduates. Department Clinical Research - The Clinical Research team is responsible for the implementation of all clinical research projects, from planning to reporting. Projects comprise clinical trials as well as all types of non-inter
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You will be responsible for defining, planning, and executing all necessary clinical studies and projects worldwide and evaluating clinical data for product definition, registration, and marketing purposes. * Responsibility for budget and timeline planning for the entire clinical strategy Oversight of statistical analysis and evaluation of clinical data Your Role As a Clinical Affairs Manager (m/f/x), you will play a pivotal role in driving the clinical strategy for the international approval of complex new product developments and product improvements in the ZEISS microsurgery. * Definition and implementation of the clinical evaluation strategy for complex and challenging development projects focused on innovative mi
You will be responsible for defining, planning, and executing all necessary clinical studies and projects worldwide and evaluating clinical data for product definition, registration, and marketing purposes. * Responsibility for budget and timeline planning for the entire clinical strategy Oversight of statistical analysis and evaluation of clinical data Your Role As a Clinical Affairs Manager (m/f/x), you will play a pivotal role in driving the clinical strategy for the international approval of complex new product developments and product improvements in the ZEISS microsurgery. * Definition and implementation of the clinical evaluation strategy for complex and challenging development projects focused on innovative mi
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Provide data management and analytics input to IT solutions supporting clinical data processing workflows - EMA relies on clinical study data submitted by medicines developers and is expanding its ability to receive and analyse individual patient level data in structured electronic formats. In this job you will Work as a Data Science Specialist supporting the receipt, validation, characterisation, analysis and visualisation of clinical study data. * Support the development of business processes for structured clinical study data received from medicines developers * Perform analyses of clinical study data to support marketing authorisa
Provide data management and analytics input to IT solutions supporting clinical data processing workflows - EMA relies on clinical study data submitted by medicines developers and is expanding its ability to receive and analyse individual patient level data in structured electronic formats. In this job you will Work as a Data Science Specialist supporting the receipt, validation, characterisation, analysis and visualisation of clinical study data. * Support the development of business processes for structured clinical study data received from medicines developers * Perform analyses of clinical study data to support marketing authorisa
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The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. Accordingly, the candidate is responsible for executing the technology transfer in accordance with the established standard processes to facilitate alignment of tech transfer and validation activities across the projects for Drug Product manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a smooth transition of projects, recommends, and implements new technologies, as needed and supports Supply Chain Management with technical issues during ...
The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. Accordingly, the candidate is responsible for executing the technology transfer in accordance with the established standard processes to facilitate alignment of tech transfer and validation activities across the projects for Drug Product manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a smooth transition of projects, recommends, and implements new technologies, as needed and supports Supply Chain Management with technical issues during ...
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Team Lead (f/m/x) Marketing Management - Workflow & Automation
Team Lead (f/m/x) Marketing Management - Workflow & Automation
Sysmex Europe SE
Hamburg
Teilweise Home-Office
What if you could play a key role in shaping the future of workflow and automation in clinical diagnostics? As Team Lead Marketing Management – Workflow & Automation (f/m/x), you drive the strategic development and implementation of marketing initiatives supporting our automation portfolio. You lead and develop a high-performing team of marketing managers and collaborate closely with Product Management, Workflow Consulting, Application Support, and regional across EMEA. * Collaborating with Product Management to support launches and lifecycle marketing - Execution & Performance Management You will thrive in this role if you bring strategic thinking, strong leadership skills, and a deep understanding of workflow and automation in clinical diagnostics. * 6+ years of exp
What if you could play a key role in shaping the future of workflow and automation in clinical diagnostics? As Team Lead Marketing Management – Workflow & Automation (f/m/x), you drive the strategic development and implementation of marketing initiatives supporting our automation portfolio. You lead and develop a high-performing team of marketing managers and collaborate closely with Product Management, Workflow Consulting, Application Support, and regional across EMEA. * Collaborating with Product Management to support launches and lifecycle marketing - Execution & Performance Management You will thrive in this role if you bring strategic thinking, strong leadership skills, and a deep understanding of workflow and automation in clinical diagnostics. * 6+ years of exp
The Director, Cell Therapy Quality Management (Dir. CT QM) role will work in a collaborative manner with other members of the Cell Therapy Clinical Operations (CTCO) Business Processes, Quality & Learning (BPQL) team in order to provide expert quality advice and coaching so as to support the successful delivery of Cell Therapy Programmes. * Process critical metrics & measurement: Support development, using quality-related data to inform process and business improvement activities. * At least 7 years of relevant operational and/or quality experience in Drug Development within a pharmaceutical or clinical background * Solid understanding of business process, technology and Clinical Study information knowledge * Demonstrated time management foresight and proven skills to
The Director, Cell Therapy Quality Management (Dir. CT QM) role will work in a collaborative manner with other members of the Cell Therapy Clinical Operations (CTCO) Business Processes, Quality & Learning (BPQL) team in order to provide expert quality advice and coaching so as to support the successful delivery of Cell Therapy Programmes. * Process critical metrics & measurement: Support development, using quality-related data to inform process and business improvement activities. * At least 7 years of relevant operational and/or quality experience in Drug Development within a pharmaceutical or clinical background * Solid understanding of business process, technology and Clinical Study information knowledge * Demonstrated time management foresight and proven skills to
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Scientific Project Manager for Governance & Regulatory Processes
Scientific Project Manager for Governance & Regulatory Processes
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
Experience with bioinformatics, research data management, or handling sensitive human or clinical data is strongly preferred - We are seeking a scientific project manager to support the GHGA office in coordinating GHGA's multi-stakeholder activities, with a focus on governance, grant management, regulatory workflows, and legal processes related to data access and operation of the GHGA. We welcome applicants with diverse academic and professional backgrounds that intersect with project management, data governance, research infrastructure, or regulatory processes. * Demonstrated experience in science and project management, research administration, regulatory affairs and legal management, and data governance, ideally within an academic environment - The German Cancer Research Center coordinates the German Human Genome-Phenome Archive (GHGA), a national research data ...
Experience with bioinformatics, research data management, or handling sensitive human or clinical data is strongly preferred - We are seeking a scientific project manager to support the GHGA office in coordinating GHGA's multi-stakeholder activities, with a focus on governance, grant management, regulatory workflows, and legal processes related to data access and operation of the GHGA. We welcome applicants with diverse academic and professional backgrounds that intersect with project management, data governance, research infrastructure, or regulatory processes. * Demonstrated experience in science and project management, research administration, regulatory affairs and legal management, and data governance, ideally within an academic environment - The German Cancer Research Center coordinates the German Human Genome-Phenome Archive (GHGA), a national research data ...
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Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) Sie agieren als zentrale Steuerungs- und Integrationsfunktion zwischen R&D, Produktmanagement, CPO, CTO sowie weiteren internen und externen Stakeholdern. * Enge Zusammenarbeit mit Produktmanagement und CPO zur Sicherstellung konsistenter Projekt-, Produkt- und Technologieziele * Einführung, Skalierung und Weiterentwicklung von Jira Premium als zentrales Projekt- und Portfoliomanagement-Tool * Mehrjährige (Senior-)Erfahrung im Projektmanagement komplexer Entwicklungs- oder Softwareprojekte, idealerweise im MedTech- oder regulierten Umfeld * Sehr gutes Verständnis klassischer und agiler Projektmanagement-Methoden (z. B. Scrum, SAFe-nahe Ansätz
Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) Sie agieren als zentrale Steuerungs- und Integrationsfunktion zwischen R&D, Produktmanagement, CPO, CTO sowie weiteren internen und externen Stakeholdern. * Enge Zusammenarbeit mit Produktmanagement und CPO zur Sicherstellung konsistenter Projekt-, Produkt- und Technologieziele * Einführung, Skalierung und Weiterentwicklung von Jira Premium als zentrales Projekt- und Portfoliomanagement-Tool * Mehrjährige (Senior-)Erfahrung im Projektmanagement komplexer Entwicklungs- oder Softwareprojekte, idealerweise im MedTech- oder regulierten Umfeld * Sehr gutes Verständnis klassischer und agiler Projektmanagement-Methoden (z. B. Scrum, SAFe-nahe Ansätz
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Strong expertise in modern molecular biology and biochemical techniques, with excellent data management skills. We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external , always with the goal of translating research outcomes directly into patient care. * Building and maintaining biobanks and databases of biomaterials and associated metadata for future analyses. * Experience integrating translational research into clinical studies.
Strong expertise in modern molecular biology and biochemical techniques, with excellent data management skills. We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external , always with the goal of translating research outcomes directly into patient care. * Building and maintaining biobanks and databases of biomaterials and associated metadata for future analyses. * Experience integrating translational research into clinical studies.
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You will shape the direction of global clinical safety, medical affairs, and pharmacovigilance - ensuring the highest standards of patient safety and scientific integrity across our vaccine portfolio. We're looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manu
You will shape the direction of global clinical safety, medical affairs, and pharmacovigilance - ensuring the highest standards of patient safety and scientific integrity across our vaccine portfolio. We're looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manu
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Research fellowships for PhD/MD candidates or Postdocs (f/d/m)
Research fellowships for PhD/MD candidates or Postdocs (f/d/m)
MHH - Medizinische Hochschule Hannover
Hannover
Cutting-edge, highly interdisciplinary implant research and implant life cycle management, from basic research to clinical application, patient and science communication - The DFG-funded Collaborative Research Centre/Transregio CRC/TRR 298 “Safety-Integrated and Infection-Reactive Implants” (SIIRI) awards 10 research fellowships for PhD/MD candidates or Postdocs in either dentistry or medicine, natural sciences, e.g. chemistry, biology and life sciences, engineering sciences, e.g. mechanical engineering, simulation and modelling or data sciences. The developed systems will merge into a digital implant life cycle management, ultimately leading to a long-term increase in implant safety.
Cutting-edge, highly interdisciplinary implant research and implant life cycle management, from basic research to clinical application, patient and science communication - The DFG-funded Collaborative Research Centre/Transregio CRC/TRR 298 “Safety-Integrated and Infection-Reactive Implants” (SIIRI) awards 10 research fellowships for PhD/MD candidates or Postdocs in either dentistry or medicine, natural sciences, e.g. chemistry, biology and life sciences, engineering sciences, e.g. mechanical engineering, simulation and modelling or data sciences. The developed systems will merge into a digital implant life cycle management, ultimately leading to a long-term increase in implant safety.
Cell Therapy Territory Operations Manager / Regional Cell Therapy Operations Lead (m/f/d)
Cell Therapy Territory Operations Manager / Regional Cell Therapy Operations Lead (m/f/d)
AstraZeneca
bundesweit
Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. It delivers operational and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation. * Drive initiatives across clinical and commercial cell therapy from development through post-market. * Partner with internal teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing).
Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. It delivers operational and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation. * Drive initiatives across clinical and commercial cell therapy from development through post-market. * Partner with internal teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing).
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Als Clinical Data Engineer sind Sie Teil eines interdisziplinären Teams, das klinische Studien durch datengestützte Lösungen voranbringt. * Weiterbildung und Entwicklungsmöglichkeiten im Bereich Clinical Data Science - Unsere Kernkompetenz liegt in der Einführung und Betreuung von Informations-Management-Systemen primär für das Dokumenten- und Qualitätsmanagement.
Als Clinical Data Engineer sind Sie Teil eines interdisziplinären Teams, das klinische Studien durch datengestützte Lösungen voranbringt. * Weiterbildung und Entwicklungsmöglichkeiten im Bereich Clinical Data Science - Unsere Kernkompetenz liegt in der Einführung und Betreuung von Informations-Management-Systemen primär für das Dokumenten- und Qualitätsmanagement.
Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. This role is part of the Oncology R&D team tasked with supporting Clinical and Commercial production across multiple sites. * Collaborate across functions with Clinical Operations, Supply Chain, Medical, IT, and Commercial teams to meet the needs of patients and healthcare providers. * Strong organizational and time management skills, especially in field-based roles requiring autonomy and adaptability. * A collaborative spirit and the ability to work effectively across diverse teams including Clinical Ops, Supply Chain, Medical, and IT. * Exposure to process improvement, training, or SOP development in clinical or operational settings.
Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. This role is part of the Oncology R&D team tasked with supporting Clinical and Commercial production across multiple sites. * Collaborate across functions with Clinical Operations, Supply Chain, Medical, IT, and Commercial teams to meet the needs of patients and healthcare providers. * Strong organizational and time management skills, especially in field-based roles requiring autonomy and adaptability. * A collaborative spirit and the ability to work effectively across diverse teams including Clinical Ops, Supply Chain, Medical, and IT. * Exposure to process improvement, training, or SOP development in clinical or operational settings.
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Chief Medical and Research Officer (CMO) / Member Executive Board (m/w/d)
Chief Medical and Research Officer (CMO) / Member Executive Board (m/w/d)
GBG Forschungs GmbH
Neu-Isenburg bei Frankfurt am Main
Teilweise Home-Office
Als Chief Medical and Research Officer übernehmen Sie die strategische und medizinisch-wissenschaftliche Leitung des Bereichs Medicine & Research, einschließlich Statistics, Translational Research und Data Management. * Arbeiten Sie eng mit den Bereichen Statistik, Data Management und translationaler Forschung zusammen, um evidenzbasierte Entscheidungen in Echtzeit zu ermöglichen. Bridging the gap between clinical excellence and operational efficiency. * Initiieren und gestalten Sie innovative Studienkonzepte, die neueste Erkenntnisse aus Data Analytics und translationaler Forschung integrieren.
Als Chief Medical and Research Officer übernehmen Sie die strategische und medizinisch-wissenschaftliche Leitung des Bereichs Medicine & Research, einschließlich Statistics, Translational Research und Data Management. * Arbeiten Sie eng mit den Bereichen Statistik, Data Management und translationaler Forschung zusammen, um evidenzbasierte Entscheidungen in Echtzeit zu ermöglichen. Bridging the gap between clinical excellence and operational efficiency. * Initiieren und gestalten Sie innovative Studienkonzepte, die neueste Erkenntnisse aus Data Analytics und translationaler Forschung integrieren.
Build proof-of-principle demonstrators & test your solution with product management and our clinical partners * Evaluate and refine your approach on real-world data
Build proof-of-principle demonstrators & test your solution with product management and our clinical partners * Evaluate and refine your approach on real-world data
It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. As a Senior Software Developer for FORUM, you are designing and developing a key health data management product for ophthalmology. You define and implement business features, technical enablers, and security concepts for a complex data management solution which runs on-Prem and in cloud. * Servant leader for java development, especially for health data management platforms - ZEISS Medical Ecosystem opens possibilities for the creation of new solutions, where data passes seamlessly from one ZEISS devi
It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. As a Senior Software Developer for FORUM, you are designing and developing a key health data management product for ophthalmology. You define and implement business features, technical enablers, and security concepts for a complex data management solution which runs on-Prem and in cloud. * Servant leader for java development, especially for health data management platforms - ZEISS Medical Ecosystem opens possibilities for the creation of new solutions, where data passes seamlessly from one ZEISS devi