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55.113 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 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 55111 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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Give insights into clinical data sets and evidence for our company's products to internal stakeholders. * Keep record of clinical initiatives, grants and data collections in the field. * Define data endpoints and sample sizes (together with clinical evaluation team and support of biostatistics) for data collections, studies and clinical initiatives. * Interpret and analyze clinical data for clinical evaluations and scientific projects, working closely with clinical evaluation team and biostatistics to ensure robust scientific conclusions. * Stay informed on evolving clinical trends, competitor data, and regulatory updates to refine our clinical strategies. To enlarge our Clinical Regulatory Affairs Team we are looking as soon as possible for a * Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest.
Give insights into clinical data sets and evidence for our company's products to internal stakeholders. * Keep record of clinical initiatives, grants and data collections in the field. * Define data endpoints and sample sizes (together with clinical evaluation team and support of biostatistics) for data collections, studies and clinical initiatives. * Interpret and analyze clinical data for clinical evaluations and scientific projects, working closely with clinical evaluation team and biostatistics to ensure robust scientific conclusions. * Stay informed on evolving clinical trends, competitor data, and regulatory updates to refine our clinical strategies. To enlarge our Clinical Regulatory Affairs Team we are looking as soon as possible for a * Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest.
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Partner closely with R&D, Product Management, Marketing, Sales and Quality Management on the strategy and to translate clinical insights into product innovation and market differentiation * Solid understanding of GDPR and clinical data protection requirements * Define and lead the global Clinical Affairs strategy for Brainlab's global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams * Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication * Ensure clinical compliance with EU MDR, FDA and other regulatory requirements * Build and maintain a strong clinical network of investigators, key opinion leaders and research partners * Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
Partner closely with R&D, Product Management, Marketing, Sales and Quality Management on the strategy and to translate clinical insights into product innovation and market differentiation * Solid understanding of GDPR and clinical data protection requirements * Define and lead the global Clinical Affairs strategy for Brainlab's global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams * Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication * Ensure clinical compliance with EU MDR, FDA and other regulatory requirements * Build and maintain a strong clinical network of investigators, key opinion leaders and research partners * Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
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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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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.
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Interdisziplinärer Austausch: Du arbeitest auf Augenhöhe mit Product, Data Science und Clinical Experts zusammen * Gestaltungsspielraum: Kurze Entscheidungswege und viel Platz für Eigeninitiative statt Micromanagement
Interdisziplinärer Austausch: Du arbeitest auf Augenhöhe mit Product, Data Science und Clinical Experts zusammen * Gestaltungsspielraum: Kurze Entscheidungswege und viel Platz für Eigeninitiative statt Micromanagement
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Our core competencies include Clinical Statistics, Translational Medicine & Biomarkers, Phase I & Pharmacokinetics/-Dynamics, Data Transparency & Disclosure Services, Health Technology Assessment and Bioinformatics. Staburo GmbH is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results. Our new sales manager will collaborate directly with senior management across all business areas including the CEOs. * Monitoring market, conducting competitive analysis, providing sales report to management, and collaborating with the marketing team * Tracking and analyzing sales metrics using quantitative data and preparing and monitoring the sales department budget
Our core competencies include Clinical Statistics, Translational Medicine & Biomarkers, Phase I & Pharmacokinetics/-Dynamics, Data Transparency & Disclosure Services, Health Technology Assessment and Bioinformatics. Staburo GmbH is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results. Our new sales manager will collaborate directly with senior management across all business areas including the CEOs. * Monitoring market, conducting competitive analysis, providing sales report to management, and collaborating with the marketing team * Tracking and analyzing sales metrics using quantitative data and preparing and monitoring the sales department budget
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Research Software Engineer / HIFIS Consultant
Research Software Engineer / HIFIS Consultant
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
Work with diverse medical data modalities, including radiological images, and clinical data, as well as AI-derived models - The Division of Medical Image Computing (MIC) is a leading research group pioneering advancements in machine learning and information processing to improve cancer patient care through systematic image data analytics. * Collaborate with to analyze requirements, design suitable software and data workflows, and support the implementation of modern, needs-oriented software engineering strategies * Experience in consulting, mentoring, requirements analysis, or project management in software development projects * Our Corporate Health Management Program offers a holistic approach to your well-being
Work with diverse medical data modalities, including radiological images, and clinical data, as well as AI-derived models - The Division of Medical Image Computing (MIC) is a leading research group pioneering advancements in machine learning and information processing to improve cancer patient care through systematic image data analytics. * Collaborate with to analyze requirements, design suitable software and data workflows, and support the implementation of modern, needs-oriented software engineering strategies * Experience in consulting, mentoring, requirements analysis, or project management in software development projects * Our Corporate Health Management Program offers a holistic approach to your well-being
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Through strong academic, clinical, and industry partnerships, as well as global networks, we translate biological insights into innovations for early detection, individualized therapies, and disease prevention. We are looking for an epidemiologist with a strong background and expertise in genetic epidemiology, molecular epidemiology, data science or bioinformatics. * planning, management and organization of epidemiologic research projects in the area of molecular and genetic epidemiology (with emphasis on omics technologies) * development of data analysis plans * data analysis of complex data from phenotyping, genotyping, sequencing and other omics sources * experience in the analysis of genetic and molecular data in large human cohort studies
Through strong academic, clinical, and industry partnerships, as well as global networks, we translate biological insights into innovations for early detection, individualized therapies, and disease prevention. We are looking for an epidemiologist with a strong background and expertise in genetic epidemiology, molecular epidemiology, data science or bioinformatics. * planning, management and organization of epidemiologic research projects in the area of molecular and genetic epidemiology (with emphasis on omics technologies) * development of data analysis plans * data analysis of complex data from phenotyping, genotyping, sequencing and other omics sources * experience in the analysis of genetic and molecular data in large human cohort studies
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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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Studienassistenz (m/w/d) in der Medizinischen Klinik und Poliklinik III
Studienassistenz (m/w/d) in der Medizinischen Klinik und Poliklinik III
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Die Stelle der Studienassistenz umfasst die Koordination und Organisation des Forschungsprojekts Transregio 205/3 – Projekt S02 „Enhancing data quality and harmonise further pre-analytical sample processes and retrieval of material“. * Organisation der Prüfmedikations-, Labor- und Materiallogistik einschließlich Geräteüberwachung, Bestandsmanagement, Labordiagnostik, Kostenabrechnung und Zahlungsüberwachung * Gute Kenntnisse wissenschaftlicher Arbeitsprozesse sowie der Good Clinical Practice (GCP) * Gesundheit: Umfangreiche Sport- und Bewegungsangebote in unserem topmodernen Fitnessstudio sowie Programme und Beratung zur mentalen Gesundheit, betriebliches Gesundheitsmanagement u. v. m.
Die Stelle der Studienassistenz umfasst die Koordination und Organisation des Forschungsprojekts Transregio 205/3 – Projekt S02 „Enhancing data quality and harmonise further pre-analytical sample processes and retrieval of material“. * Organisation der Prüfmedikations-, Labor- und Materiallogistik einschließlich Geräteüberwachung, Bestandsmanagement, Labordiagnostik, Kostenabrechnung und Zahlungsüberwachung * Gute Kenntnisse wissenschaftlicher Arbeitsprozesse sowie der Good Clinical Practice (GCP) * 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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Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
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.
NEU
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Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. • Maintain data quality. Timely enter and correct data into databases and reports. Analyze the data from the department's IT applications. Bachelor's Degree or Equivalent in in engineering sciences, information systems or business analysis or another field relevant to the position, 8 years years experience of experience in consultancy and/or project management Required or - Master's Degree or equivalent in in engineering sciences, information systems or business analysis or another field relevant to the position, 6 years years experience of experience in consultancy and/or project management Required • Proven successful project management skills
Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. • Maintain data quality. Timely enter and correct data into databases and reports. Analyze the data from the department's IT applications. Bachelor's Degree or Equivalent in in engineering sciences, information systems or business analysis or another field relevant to the position, 8 years years experience of experience in consultancy and/or project management Required or - Master's Degree or equivalent in in engineering sciences, information systems or business analysis or another field relevant to the position, 6 years years experience of experience in consultancy and/or project management Required • Proven successful project management skills
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Product Expert / Analytical Process Manager (m/f/d) - 2 year contract
Product Expert / Analytical Process Manager (m/f/d) - 2 year contract
Rentschler Biopharma SE
Laupheim
Teilweise Home-Office
We are seeking a candidate with strong expertise in either immunology and/or clinical studies, including knowledge of safety profiles of biopharmaceuticals, or a solid understanding of protein chemistry at the molecular level. In both cases, a strong ability to interpret and communicate complex analytical data is essential * Health: Corporate health management, company doctor
We are seeking a candidate with strong expertise in either immunology and/or clinical studies, including knowledge of safety profiles of biopharmaceuticals, or a solid understanding of protein chemistry at the molecular level. In both cases, a strong ability to interpret and communicate complex analytical data is essential * Health: Corporate health management, company doctor
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.
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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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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 ...
NEU
The overarching goal is to gain fundamental insights into the molecular and cellular principles that underlie protective B cell immune responses and to translate our findings into clinical application. Data analysis and visualization using Excel, Prism, and PowerPoint is expected. * Our Corporate Health Management Program offers a holistic approach to your well-being
The overarching goal is to gain fundamental insights into the molecular and cellular principles that underlie protective B cell immune responses and to translate our findings into clinical application. Data analysis and visualization using Excel, Prism, and PowerPoint is expected. * Our Corporate Health Management Program offers a holistic approach to your well-being
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. * Excellent 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. * Excellent analytical skills, data-driven mindset
PhD Position (m/f/d) - Computational Biology & Single-Cell Genomics - Decoding Brain Development
PhD Position (m/f/d) - Computational Biology & Single-Cell Genomics - Decoding Brain Development
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Analysis and interpretation of high-resolution single-cell RNA-seq and scATAC-seq data to elucidate cellular processes * Processing and integration of spatial transcriptomics data to reveal molecular patterns in their tissue context * Development, optimization, and application of bioinformatic pipelines for data integration, analysis, and visualization of complex datasets * Experience in the analysis of single-cell genomics data, ideally using tools such as Seurat or Scanpy - at the Institute of Clinical Genetics * Health & Well-being: Access to modern sports and exercise programs at our health center, mental health initiatives, and comprehensive occupational health management
Analysis and interpretation of high-resolution single-cell RNA-seq and scATAC-seq data to elucidate cellular processes * Processing and integration of spatial transcriptomics data to reveal molecular patterns in their tissue context * Development, optimization, and application of bioinformatic pipelines for data integration, analysis, and visualization of complex datasets * Experience in the analysis of single-cell genomics data, ideally using tools such as Seurat or Scanpy - at the Institute of Clinical Genetics * Health & Well-being: Access to modern sports and exercise programs at our health center, mental health initiatives, and comprehensive occupational health management
PhD Position (m/f/d) in Developmental Neuroscience
PhD Position (m/f/d) in Developmental Neuroscience
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Analyzing and interpreting single-cell genomics data to investigate cellular mechanisms * Knowledge of omics data analysis (e.g., single-cell genomics) at the Institute of Clinical Genetics * Health & Well-being: Access to modern sports and exercise programs at our health center, mental health initiatives, and comprehensive occupational health management
Analyzing and interpreting single-cell genomics data to investigate cellular mechanisms * Knowledge of omics data analysis (e.g., single-cell genomics) at the Institute of Clinical Genetics * Health & Well-being: Access to modern sports and exercise programs at our health center, mental health initiatives, and comprehensive occupational health management