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- Medizinischer Dienst
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- Dresden
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51.573 Treffer für Clinical Data Management Jobs in Westliches Europa im Umkreis von 30 km
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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 in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis * Advising on and contributing to the development of new tools and methodologies for clinical trial analytics ...
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 in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis * Advising on and contributing to the development of new tools and methodologies for clinical trial analytics ...
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Group Leader – Clinical Operational Excellence (m|f|d)
Group Leader – Clinical Operational Excellence (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
In this leadership position, you will collaborate closely with Clinical Trial Management, Data Management, QA, and vendors, providing structured leadership through goal setting, coaching, and performance reviews. * Together with your team you will oversee TMF services, trial oversight- and training requirements for clinical studies, including Key Peformance Indicator management, TMF vendor oversight, and proactive risk mitigation. * You are a strong and experienced leader with proven disciplinary and functional management skills, demonstrating excellent organizational abilities and fostering collaboration across clinical teams and vendors. 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.
In this leadership position, you will collaborate closely with Clinical Trial Management, Data Management, QA, and vendors, providing structured leadership through goal setting, coaching, and performance reviews. * Together with your team you will oversee TMF services, trial oversight- and training requirements for clinical studies, including Key Peformance Indicator management, TMF vendor oversight, and proactive risk mitigation. * You are a strong and experienced leader with proven disciplinary and functional management skills, demonstrating excellent organizational abilities and fostering collaboration across clinical teams and vendors. 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.
Noch nichts dabei? Es gibt 51571 weitere Jobs, die zu deiner Suche passen könnten
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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 microsurgical applications in the area of intra-operative visualization and digital imaging in neurosurgery
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 microsurgical applications in the area of intra-operative visualization and digital imaging in neurosurgery
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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 über erste Kenntnisse im Bereich Studiendesign, Studienprotokollen, GCP (Good Clinical Practice) und den relevanten regulatorischen Anforderungen (ICH-GCP, 21 CFR Part 11)
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 über erste Kenntnisse im Bereich Studiendesign, Studienprotokollen, GCP (Good Clinical Practice) und den relevanten regulatorischen Anforderungen (ICH-GCP, 21 CFR Part 11)
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Specialist Regulatory Data Management (m/w/d)
Specialist Regulatory Data Management (m/w/d)
Pajunk GmbH Medizintechnologie
Geisingen
Teilweise Home-Office
Unterstützen Sie unser Team in Geisingen zum nächstmöglichen Zeitpunkt als Specialist Regulatory Data Management (m/w/d). * Koordination und Abstimmung mit unterschiedlichen internen Bereichen, vor allem IT, QM, Marketing und Clinical Affairs
Unterstützen Sie unser Team in Geisingen zum nächstmöglichen Zeitpunkt als Specialist Regulatory Data Management (m/w/d). * Koordination und Abstimmung mit unterschiedlichen internen Bereichen, vor allem IT, QM, Marketing und Clinical Affairs
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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-interventional healthcare research. * Cross-functional Leadership & Compliance: Align research, quality, regulatory, legal and commercial stakeholders, consider interests and inputs from ...
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-interventional healthcare research. * Cross-functional Leadership & Compliance: Align research, quality, regulatory, legal and commercial stakeholders, consider interests and inputs from ...
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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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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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Manage key processes in the collection and maintenance of provider related data in collaboration with the Network Services Team, Clinical Quality Team, Site Assessment Team and Medical Teams * Establish the engagement strategy for own portfolio, based on the regional/country strategy developed by the Network Management Team with the purpose of reaching the contractual objectives related to the host nation providers, focused with priority on reaching the medical record collection KPIs and the Network coverage and accuracy objectives and requirements * Proven service delivery experience in a professional services B2B environment or senior account management experience or program management experience * Previous exposure to healthcare and healthcare provider management a plus * Proven experience in building strong and effective relationships with at medical institutions – including ...
Manage key processes in the collection and maintenance of provider related data in collaboration with the Network Services Team, Clinical Quality Team, Site Assessment Team and Medical Teams * Establish the engagement strategy for own portfolio, based on the regional/country strategy developed by the Network Management Team with the purpose of reaching the contractual objectives related to the host nation providers, focused with priority on reaching the medical record collection KPIs and the Network coverage and accuracy objectives and requirements * Proven service delivery experience in a professional services B2B environment or senior account management experience or program management experience * Previous exposure to healthcare and healthcare provider management a plus * Proven experience in building strong and effective relationships with at medical institutions – including ...
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Clinician Scientist (m/w/d) Medizinische Klinik und Poliklinik 1 - Hämatologie
Clinician Scientist (m/w/d) Medizinische Klinik und Poliklinik 1 - Hämatologie
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Die Stelle ist an das intramurale ForwarDD Clinician Scientist Programm der Dresden School of Clinical Science angebunden, das unter anderem ein strukturiertes Curriculum, Mentoring sowie den Austausch mit anderen Clinician Scientists bietet. * Interdisziplinäre Zusammenarbeit mit Expert*innen aus Medizin, Informatik, Bioinformatik und Data Science * Gesundheit: Umfangreiche Sport- und Bewegungsangebote in unserem topmodernen Fitnessstudio sowie Programme und Beratung zur mentalen Gesundheit, betriebliches Gesundheitsmanagement u. v. m.
Die Stelle ist an das intramurale ForwarDD Clinician Scientist Programm der Dresden School of Clinical Science angebunden, das unter anderem ein strukturiertes Curriculum, Mentoring sowie den Austausch mit anderen Clinician Scientists bietet. * Interdisziplinäre Zusammenarbeit mit Expert*innen aus Medizin, Informatik, Bioinformatik und Data Science * Gesundheit: Umfangreiche Sport- und Bewegungsangebote in unserem topmodernen Fitnessstudio sowie Programme und Beratung zur mentalen Gesundheit, betriebliches Gesundheitsmanagement u. v. m.
NEU
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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 Ansätze) * Erfahrung in der Einführung und Skalierung von Projekt- und Portfoliomanagement-Strukturen, idealerweise mit Jira Premium
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 Ansätze) * Erfahrung in der Einführung und Skalierung von Projekt- und Portfoliomanagement-Strukturen, idealerweise mit Jira Premium
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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.
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Overseeing the creation, operation, and maintenance of real-world test environments and clinical-grade validation labs * Fostering strong collaboration with Software Engineering, Product Management, and regional and global QA stakeholders * Communicating quality metrics, risks, and improvement initiatives clearly and transparently to senior management and key stakeholders * A confident leadership style combined with excellent communication and stakeholder management skills * Experience with AI/ML technologies and data-driven healthcare applications is an advantage - In-house gym, various sports courses, massages, company medical and psychological care, workplace glasses, general health management
Overseeing the creation, operation, and maintenance of real-world test environments and clinical-grade validation labs * Fostering strong collaboration with Software Engineering, Product Management, and regional and global QA stakeholders * Communicating quality metrics, risks, and improvement initiatives clearly and transparently to senior management and key stakeholders * A confident leadership style combined with excellent communication and stakeholder management skills * Experience with AI/ML technologies and data-driven healthcare applications is an advantage - In-house gym, various sports courses, massages, company medical and psychological care, workplace glasses, general health management
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You'll lead a growing, cross-functional design team across Product, Content, Pathway, CRM, Clinical, and Engineering, building a scalable, intelligent, and personalised experience powered by our Behaviour Change Engine. * Collaborate cross-functionally with product, clinical, and engineering teams to align on strategy and user needs. * Champion measurable impact - using data, OKRs, and usability validation to drive patient engagement and health outcomes. * Excellent stakeholder management and communication skills - you challenge PMs and influence at executive level.
You'll lead a growing, cross-functional design team across Product, Content, Pathway, CRM, Clinical, and Engineering, building a scalable, intelligent, and personalised experience powered by our Behaviour Change Engine. * Collaborate cross-functionally with product, clinical, and engineering teams to align on strategy and user needs. * Champion measurable impact - using data, OKRs, and usability validation to drive patient engagement and health outcomes. * Excellent stakeholder management and communication skills - you challenge PMs and influence at executive level.
Steering of relevant project partners for launch campaigns: you will work with product management, communication departments and clinical regulatory stakeholders to steer and implement integrated marketing plans for global launches - You will collaborate closely with the global and local organizations, particularly in growth markets, in order to address customers' needs (surgeons, clinical staff) to further drive business growth of ZEISS SMILE pro. * Development and definition of product launch plans: In constant communication with markets and product management you will act as a team and define product launch plans for workflows and products. * Minimum of 5 years of work experience in Marketing, preferably in Ophthalmology or at least in HealthcareExcellent analytical skills, data-driven mindset
Steering of relevant project partners for launch campaigns: you will work with product management, communication departments and clinical regulatory stakeholders to steer and implement integrated marketing plans for global launches - You will collaborate closely with the global and local organizations, particularly in growth markets, in order to address customers' needs (surgeons, clinical staff) to further drive business growth of ZEISS SMILE pro. * Development and definition of product launch plans: In constant communication with markets and product management you will act as a team and define product launch plans for workflows and products. * Minimum of 5 years of work experience in Marketing, preferably in Ophthalmology or at least in HealthcareExcellent analytical skills, data-driven mindset
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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, Manufacturing/CMC, Quality, Commercial, and Market Access
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, Manufacturing/CMC, Quality, Commercial, and Market Access
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Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. * Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. * Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure ...
Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. * Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. * Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure ...
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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.
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(Senior) Product Support Specialist – Cranial & Functional Planning Applications
(Senior) Product Support Specialist – Cranial & Functional Planning Applications
Brainlab
München
Teilweise Home-Office
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. * Experience with medical image data stored in DICOM (Digital Imaging and Communications in Medicine) standard
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. * Experience with medical image data stored in DICOM (Digital Imaging and Communications in Medicine) standard
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Lifecare Germany GmbH, part of the Lifecare Group, is a clinical-stage medical sensor company developing advanced technologies for the sensing and monitoring of various body analytes. The German entity in Mainz is responsible for key development tasks including sensor design, chemistry validation, system evaluation and data analysis from both laboratory and patient studies. In addition to R&D, our laboratory provides commercial services for the pharmaceutical and biotechnology industries, supporting clinical research, testing and approval processes for drugs and medical devices, as well as general laboratory services for medical institutions. * Data acquisition and preparation * Evaluation and analysis of data * Collaboration in the development of methods for data analysis and evaluation * Independent work in various projects, according to common priorities in the field of ...
Lifecare Germany GmbH, part of the Lifecare Group, is a clinical-stage medical sensor company developing advanced technologies for the sensing and monitoring of various body analytes. The German entity in Mainz is responsible for key development tasks including sensor design, chemistry validation, system evaluation and data analysis from both laboratory and patient studies. In addition to R&D, our laboratory provides commercial services for the pharmaceutical and biotechnology industries, supporting clinical research, testing and approval processes for drugs and medical devices, as well as general laboratory services for medical institutions. * Data acquisition and preparation * Evaluation and analysis of data * Collaboration in the development of methods for data analysis and evaluation * Independent work in various projects, according to common priorities in the field of ...
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Medical Writer (m/w/d) Market Access - Hannover, Germany (Hybride)
Medical Writer (m/w/d) Market Access - Hannover, Germany (Hybride)
SKC Beratungsgesellschaft mbH
Hannover
Teilweise Home-Office
Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research * Advanced skills in MS-Office CRM, project management, and data tools (preferred), knowledge of LaTeX is an advantage * Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results * Excellent organizational, agile and classic project management skills
Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research * Advanced skills in MS-Office CRM, project management, and data tools (preferred), knowledge of LaTeX is an advantage * Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results * Excellent organizational, agile and classic project management skills
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 device to another using artificial-intelligence-powered applications and software tools.
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 device to another using artificial-intelligence-powered applications and software tools.
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
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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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Proven experience in project and/or operations management within the clinical trial industry, ideally in a leadership role. Clariness is looking for a Team Lead Project and Operations Management (f/m/d) based in Berlin or Hamburg. In this role you will be responsible for leading and ensuring the successful delivery of clinical trial recruitment projects across multiple studies and clients. * Leading and supporting to ensure smooth and timely delivery of clinical trial recruitment projects. * Excellent communication and stakeholder management skills. * Good understanding of project management methodologies and tools. * Experience with performance metrics, portfolio reporting, and data-driven decision-making. * Project management certifications (e.g. PMP, PRINCE2) are a plus. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially ...
Proven experience in project and/or operations management within the clinical trial industry, ideally in a leadership role. Clariness is looking for a Team Lead Project and Operations Management (f/m/d) based in Berlin or Hamburg. In this role you will be responsible for leading and ensuring the successful delivery of clinical trial recruitment projects across multiple studies and clients. * Leading and supporting to ensure smooth and timely delivery of clinical trial recruitment projects. * Excellent communication and stakeholder management skills. * Good understanding of project management methodologies and tools. * Experience with performance metrics, portfolio reporting, and data-driven decision-making. * Project management certifications (e.g. PMP, PRINCE2) are a plus. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially ...
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