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1.855 Treffer für Clinical Development Jobs
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The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Director of Computational Pathology Delivery Operations (m/f/d) in Munich to lead the execution of Computational Pathology (CP) workflows across AI/ML development, biomarker discovery, and diagnostic readiness in a cross-functional environment. * Provide direct line management for >10 CP Delivery Managers embedded across drug programs and ...
The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Director of Computational Pathology Delivery Operations (m/f/d) in Munich to lead the execution of Computational Pathology (CP) workflows across AI/ML development, biomarker discovery, and diagnostic readiness in a cross-functional environment. * Provide direct line management for >10 CP Delivery Managers embedded across drug programs and ...
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Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * As a member of the German Corporate Affairs teams, you contribute to the development of annual patient advocacy strategy, goals and patient engagement plans, aligning within Corporate Affairs for Germany and ensure execution per therapeutic area * Conceptualize and coordinate engagement of PAOs in the development of local Patient Support Programs (PSPs) working in close partnership with the Patient Medical Program team and local medical team responsible for PSPs
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * As a member of the German Corporate Affairs teams, you contribute to the development of annual patient advocacy strategy, goals and patient engagement plans, aligning within Corporate Affairs for Germany and ensure execution per therapeutic area * Conceptualize and coordinate engagement of PAOs in the development of local Patient Support Programs (PSPs) working in close partnership with the Patient Medical Program team and local medical team responsible for PSPs
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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 have industry experience in Pharma/Biotech, ideally in a cross-functional, global clinical development setting. 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 the successful planning, execution, and supervision of clinical trials in hemato-oncology.
You have industry experience in Pharma/Biotech, ideally in a cross-functional, global clinical development setting. 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 the successful planning, execution, and supervision of clinical trials in hemato-oncology.
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The Clinical Workflow Manager (CWM) - Bioprocessing is responsible for Driving the integration of Cytiva technologies by targeting drugs in clinical development. * Qualify customer needs with a focus on target molecules in preclinical, phase 1, and phase 2 of molecule development, using a workflow-centric approach. Acting as a Process Development Subject Matter Expert (SME) both internally and externally - Collaborate with (AM), Sales Specialists (SS), and Field Application Specialists (FAS) for technical support to meet customer and process development requirements. * Upstream and downstream process development experience * Strong understanding of process development
The Clinical Workflow Manager (CWM) - Bioprocessing is responsible for Driving the integration of Cytiva technologies by targeting drugs in clinical development. * Qualify customer needs with a focus on target molecules in preclinical, phase 1, and phase 2 of molecule development, using a workflow-centric approach. Acting as a Process Development Subject Matter Expert (SME) both internally and externally - Collaborate with (AM), Sales Specialists (SS), and Field Application Specialists (FAS) for technical support to meet customer and process development requirements. * Upstream and downstream process development experience * Strong understanding of process development
Noch nichts dabei? Es gibt 1851 weitere Jobs, die zu deiner Suche passen könnten
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Project Coordinator / Data Steward in Clinical Research (f/m/x) Biomedizinische Informatik – Datenintegrationszentrum
Project Coordinator / Data Steward in Clinical Research (f/m/x) Biomedizinische Informatik – Datenintegrationszentrum
Universitätsklinikum Köln (AöR)
Köln
Teilweise Home-Office
In this responsible position, you will play a key role in making routine medical data available for clinical research and in managing the development and implementation of innovative IT solutions in healthcare. Your role focuses on advancing the digital transformation of the Medical Data Integration Centre by coordinating knowledge exchange on the intersection of research, IT, and clinical teams, managing national and international collaborations and making significant contributions to the further development of data-based medicine at the University Hospital of Cologne. * Establishing data protection guidelines for secondary use of patient-sensitive data in clinical research and further development of data standards - Project Coordinator / Data Steward in Clinical Research (f/m/x) * Extraction and preparation of data from clinical information systems for research projects
In this responsible position, you will play a key role in making routine medical data available for clinical research and in managing the development and implementation of innovative IT solutions in healthcare. Your role focuses on advancing the digital transformation of the Medical Data Integration Centre by coordinating knowledge exchange on the intersection of research, IT, and clinical teams, managing national and international collaborations and making significant contributions to the further development of data-based medicine at the University Hospital of Cologne. * Establishing data protection guidelines for secondary use of patient-sensitive data in clinical research and further development of data standards - Project Coordinator / Data Steward in Clinical Research (f/m/x) * Extraction and preparation of data from clinical information systems for research projects
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For the Aesculap division at our Tuttlingen location, we are looking for a Business Development Manager (f/m/d) for Robotic Surgery within our Global Marketing department. * You identify, build, and maintain strong relationships with international to support strategic market development and long-term business success * You provide operational support to assigned regions and actively drive long-term strategic business development in alignment with overall company objectives * As a Business Development Manager (f/m/d) you play a key role in shaping and expanding the Robotic Surgery business by contributing to the development of scalable sales structures, processes, and market approaches * You provide professional instruction in Robotic Surgery and support local business planning by offering strategic guidance across relevant clinical and commercial topics
For the Aesculap division at our Tuttlingen location, we are looking for a Business Development Manager (f/m/d) for Robotic Surgery within our Global Marketing department. * You identify, build, and maintain strong relationships with international to support strategic market development and long-term business success * You provide operational support to assigned regions and actively drive long-term strategic business development in alignment with overall company objectives * As a Business Development Manager (f/m/d) you play a key role in shaping and expanding the Robotic Surgery business by contributing to the development of scalable sales structures, processes, and market approaches * You provide professional instruction in Robotic Surgery and support local business planning by offering strategic guidance across relevant clinical and commercial topics
Is it time to move away from the demands of clinical care? This is a fantastic opportunity for nurses to move away from the demands of a clinical environment to an on-site case manager role using their medical expertise. * The nurse would provide comprehensive in-patient clinical case management in line with clinical and Intl. * Liaise with patients to obtain detailed clinical information including past medical history to allow for accurate on-going case management * Hybrid approach blending clinical visits and remote responsibilities - If you enjoy autonomy, variety, and meaningful clinical interaction, this is the nursing role you have been looking for. * A unique clinical role outside the traditional hospital environment * Clear career pathways and professional development opportunities
Is it time to move away from the demands of clinical care? This is a fantastic opportunity for nurses to move away from the demands of a clinical environment to an on-site case manager role using their medical expertise. * The nurse would provide comprehensive in-patient clinical case management in line with clinical and Intl. * Liaise with patients to obtain detailed clinical information including past medical history to allow for accurate on-going case management * Hybrid approach blending clinical visits and remote responsibilities - If you enjoy autonomy, variety, and meaningful clinical interaction, this is the nursing role you have been looking for. * A unique clinical role outside the traditional hospital environment * Clear career pathways and professional development opportunities
Is it time to move away from the demands of clinical care? This is a fantastic opportunity for nurses to move away from the demands of a clinical environment to an on-site case manager role using their medical expertise. * The nurse would provide comprehensive in-patient clinical case management in line with clinical and Intl. * Liaise with patients to obtain detailed clinical information including past medical history to allow for accurate on-going case management * Hybrid approach blending clinical visits and remote responsibilities - If you enjoy autonomy, variety, and meaningful clinical interaction, this is the nursing role you have been looking for. * A unique clinical role outside the traditional hospital environment * Clear career pathways and professional development opportunities
Is it time to move away from the demands of clinical care? This is a fantastic opportunity for nurses to move away from the demands of a clinical environment to an on-site case manager role using their medical expertise. * The nurse would provide comprehensive in-patient clinical case management in line with clinical and Intl. * Liaise with patients to obtain detailed clinical information including past medical history to allow for accurate on-going case management * Hybrid approach blending clinical visits and remote responsibilities - If you enjoy autonomy, variety, and meaningful clinical interaction, this is the nursing role you have been looking for. * A unique clinical role outside the traditional hospital environment * Clear career pathways and professional development opportunities
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Postdoctoral Scientist in Translational Bioinformatics and Pharmacogenomics
Postdoctoral Scientist in Translational Bioinformatics and Pharmacogenomics
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
The goal of the NCT is to bring promising results from cancer research into clinical application quickly and safely. You will evaluate molecular biomarkers for the inclusion of patients in interventional clinical trials. Furthermore, you may participate in the development of workflows and pipelines for the analysis of high-dimensional data. * Experience in the analysis of next-generation sequencing data, ideally in a clinical context, in interpreting actionable mutations, or in genotyping pharmacogenes * Develop your full potential: access to the DKFZ International Postdoc Program and DKFZ Career Service with targeted offers for your personal development to further develop your talents
The goal of the NCT is to bring promising results from cancer research into clinical application quickly and safely. You will evaluate molecular biomarkers for the inclusion of patients in interventional clinical trials. Furthermore, you may participate in the development of workflows and pipelines for the analysis of high-dimensional data. * Experience in the analysis of next-generation sequencing data, ideally in a clinical context, in interpreting actionable mutations, or in genotyping pharmacogenes * Develop your full potential: access to the DKFZ International Postdoc Program and DKFZ Career Service with targeted offers for your personal development to further develop your talents
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The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for investigational and marketed products and he ensures that regulatory/competitive intelligence, or scientific/regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. * Identifying the need and obtaining regulatory intelligence, researching precedent approvals and prior health authority decisions to assess applicability to support development of strategic options for assigned Otsuka products * Designing programs for complete and accurate IND/CTA/NDA/MAA and other submissions and ensuring that clinical trials are designed to meet regulatory requirements * Supporting development of strategies, drafts responses, and/or reviewing responses and documents intended for submission to ...
The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for investigational and marketed products and he ensures that regulatory/competitive intelligence, or scientific/regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. * Identifying the need and obtaining regulatory intelligence, researching precedent approvals and prior health authority decisions to assess applicability to support development of strategic options for assigned Otsuka products * Designing programs for complete and accurate IND/CTA/NDA/MAA and other submissions and ensuring that clinical trials are designed to meet regulatory requirements * Supporting development of strategies, drafts responses, and/or reviewing responses and documents intended for submission to ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Senior Specialist in Computational Pathology Delivery Operations (m/f/d) in Munich to support the execution of computational pathology workflows across AI/ML model development and biomarker discovery programs. The position plays a key role in ensuring that imaging data, metadata, annotations, and analysis outputs are fit for purpose for AI development, scientific decision-making, and potential regulatory applications. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Senior Specialist in Computational Pathology Delivery Operations (m/f/d) in Munich to support the execution of computational pathology workflows across AI/ML model development and biomarker discovery programs. The position plays a key role in ensuring that imaging data, metadata, annotations, and analysis outputs are fit for purpose for AI development, scientific decision-making, and potential regulatory applications. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, ...
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Quality Assurance Lead Nurse (m/w/d)
Quality Assurance Lead Nurse (m/w/d)
International SOS
Stuttgart, Kaiserslautern, Wiesbaden, Spangdahlem
You'll lead quality initiatives, oversee service recovery processes, analyse provider outcome data, and support audits, credentialing, and corrective action planning to uphold the TRICARE Overseas Program's clinical quality standards. * Responsible for driving support for the Clinical Management Program / Clinical Quality Oversight Plan through the collection, collation and analysis of provider level data relating to the quality outcome program. * Support provider visits to develop relationships with the quality team, to support site assessment visits and to drive the regular update of clinical outcome data from providers. * In consultation with the Clinical Quality Assurance and Innovation Lead and the Head of Clinical Quality define, implement, and administer key service quality guidelines and procedures. * Conduct regular internal reviews on service delivery through case reviews and ...
You'll lead quality initiatives, oversee service recovery processes, analyse provider outcome data, and support audits, credentialing, and corrective action planning to uphold the TRICARE Overseas Program's clinical quality standards. * Responsible for driving support for the Clinical Management Program / Clinical Quality Oversight Plan through the collection, collation and analysis of provider level data relating to the quality outcome program. * Support provider visits to develop relationships with the quality team, to support site assessment visits and to drive the regular update of clinical outcome data from providers. * In consultation with the Clinical Quality Assurance and Innovation Lead and the Head of Clinical Quality define, implement, and administer key service quality guidelines and procedures. * Conduct regular internal reviews on service delivery through case reviews and ...
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At our office location in Heilbronn, with around 100 employees, we consolidate central functions such as administration, marketing, research and development for disposables, technical service, laboratory operations, human resources, and quality. In this role, you will lead the ECMO business in international markets, drive market development, strengthen partnerships, and support regional sales teams in achieving sustainable growth. * Build, lead, and develop an international team to achieve sales and market development goals * Own regional responsibility for ECMO business development in EMEA, Eastern Europe, and Latin America, including assigned product partners * Drive revenue growth and sustainable business development with both existing and new sales partners * Solid knowledge of ECMO technologies and clinical/market requirements
At our office location in Heilbronn, with around 100 employees, we consolidate central functions such as administration, marketing, research and development for disposables, technical service, laboratory operations, human resources, and quality. In this role, you will lead the ECMO business in international markets, drive market development, strengthen partnerships, and support regional sales teams in achieving sustainable growth. * Build, lead, and develop an international team to achieve sales and market development goals * Own regional responsibility for ECMO business development in EMEA, Eastern Europe, and Latin America, including assigned product partners * Drive revenue growth and sustainable business development with both existing and new sales partners * Solid knowledge of ECMO technologies and clinical/market requirements
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Senior Specialist in Computational Pathology Delivery Operations (m/f/d) in Munich to support the execution of computational pathology workflows across AI/ML model development and biomarker discovery programs. The position plays a key role in ensuring that imaging data, metadata, annotations, and analysis outputs are fit for purpose for AI development, scientific decision-making, and potential regulatory applications. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. We are seeking a Senior Specialist in Computational Pathology Delivery Operations (m/f/d) in Munich to support the execution of computational pathology workflows across AI/ML model development and biomarker discovery programs. The position plays a key role in ensuring that imaging data, metadata, annotations, and analysis outputs are fit for purpose for AI development, scientific decision-making, and potential regulatory applications. * Manage and integrate multi-source datasets, including digital pathology images, sample metadata, ...
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Bachelor's degree or higher degree (University, FH) in Life Sciences, Public Health, Health Economics, or Clinical Research * Excellent scientific writing skills, including experience with AI-assisted content development tools
Bachelor's degree or higher degree (University, FH) in Life Sciences, Public Health, Health Economics, or Clinical Research * Excellent scientific writing skills, including experience with AI-assisted content development tools
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You own our applicative and clinical understanding of cranial tumor microsurgery procedures, you observe current trends and developments in clinics and industry - In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. * As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in cranial tumor microsurgery * You contribute with value and actively drive the workflow solution concept in product generation projects, in (early) innovation projects as well as in clinical or medical studies
You own our applicative and clinical understanding of cranial tumor microsurgery procedures, you observe current trends and developments in clinics and industry - In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. * As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in cranial tumor microsurgery * You contribute with value and actively drive the workflow solution concept in product generation projects, in (early) innovation projects as well as in clinical or medical studies
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions. Based in Munich and reporting to of Business Development, Jens Hohnwald, you'll lead a high-performing team to win new clients, expand into new verticals, and sustain our exceptional growth trajectory. You'll ultimately drive regional growth, balancing team development with hands-on deal execution. * 5+ years of hands-on experience in new business development sales, with at least 2 years of outbound sales managerial experience * Investment in external learning and development activities * Guidance in Personal Development Plan creation
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions. Based in Munich and reporting to of Business Development, Jens Hohnwald, you'll lead a high-performing team to win new clients, expand into new verticals, and sustain our exceptional growth trajectory. You'll ultimately drive regional growth, balancing team development with hands-on deal execution. * 5+ years of hands-on experience in new business development sales, with at least 2 years of outbound sales managerial experience * Investment in external learning and development activities * Guidance in Personal Development Plan creation
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Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. * Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, ...
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. * Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. * Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, ...
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Manager Liability Insurance Lines (m/f/d)
Manager Liability Insurance Lines (m/f/d)
Fresenius Medical Care Deutschland GmbH
Bad Homburg bei Frankfurt
Accountable for dedicated Insurance lines, e.g. clinical trials * Responsible for the collection of risk information for the respective insurance lines and claims * Individual opportunities for self-determined career planning and professional development
Accountable for dedicated Insurance lines, e.g. clinical trials * Responsible for the collection of risk information for the respective insurance lines and claims * Individual opportunities for self-determined career planning and professional development
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As a Project Manager in the Clinical Operations team you will independently oversee (inter-)national clinical drug trials, non-interventional studies, medical-device studies and IT-related research projects of high complexity. This role blends traditional clinical project management with the operational coordination of digital tools, platforms and IT services used in patient-centric studies. * Serve as the primary point of contact for the sponsor and drive project planning, execution and timelines - from study-start activities through ongoing study management to the coordination of all phases of the clinical-trial lifecycle. * Coordinate and manage IT services and platforms that support clinical studies (e.g., ePRO, eCOA, eCRF, patient-engagement tools). * Translate Clinical Operations requirements into technical specifications for internal and external IT teams.
As a Project Manager in the Clinical Operations team you will independently oversee (inter-)national clinical drug trials, non-interventional studies, medical-device studies and IT-related research projects of high complexity. This role blends traditional clinical project management with the operational coordination of digital tools, platforms and IT services used in patient-centric studies. * Serve as the primary point of contact for the sponsor and drive project planning, execution and timelines - from study-start activities through ongoing study management to the coordination of all phases of the clinical-trial lifecycle. * Coordinate and manage IT services and platforms that support clinical studies (e.g., ePRO, eCOA, eCRF, patient-engagement tools). * Translate Clinical Operations requirements into technical specifications for internal and external IT teams.
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions. We seek a proven sales leader with a track record of methodical team development, hands-on coaching and a high level of personal excellence. You'll drive regional growth by balancing team development with hands-on deal execution. * 5+ years of hands-on experience in new business development sales, with at least 2 years of outbound sales managerial experience * Investment in external learning and development activities * Guidance in Personal Development Plan creation
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions. We seek a proven sales leader with a track record of methodical team development, hands-on coaching and a high level of personal excellence. You'll drive regional growth by balancing team development with hands-on deal execution. * 5+ years of hands-on experience in new business development sales, with at least 2 years of outbound sales managerial experience * Investment in external learning and development activities * Guidance in Personal Development Plan creation
Our goal is to comprehensively study the impact of gene fusions and other genetic drivers in sarcomagenesis, uncover specific vulnerabilities they create, and ultimately aim at maximizing the potential for rapid clinical translation. * Unleash your full potential: targeted offers for your personal development promote your talents
Our goal is to comprehensively study the impact of gene fusions and other genetic drivers in sarcomagenesis, uncover specific vulnerabilities they create, and ultimately aim at maximizing the potential for rapid clinical translation. * Unleash your full potential: targeted offers for your personal development promote your talents
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Research at the CRTD focuses on regenerative and stem cell research ranging from basic research to application in a clinical-translational context. Using a combination of approaches the group will investigate the link between development, regeneration and degeneration of the biocrystal (otoconia) in the vertebrate inner ear at the structural, genetic, cellular and organismal level. * being an integral part of the team and the development of the group
Research at the CRTD focuses on regenerative and stem cell research ranging from basic research to application in a clinical-translational context. Using a combination of approaches the group will investigate the link between development, regeneration and degeneration of the biocrystal (otoconia) in the vertebrate inner ear at the structural, genetic, cellular and organismal level. * being an integral part of the team and the development of the group
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In this role, you will help shape the next generation of our medical software solutions and work at the intersection of customers, market, technology, and development. You will take on strategic responsibilities in upstream product management while closely collaborating on the execution and development of our digital products. o Analyze user requirements, clinical and fitness workflows, market trends, and competitive landscapes. * Drive software development from concept to market * Strong understanding of agile development practices and experience working with software engineering and UX/UI teams. * Ability to convert complex technical and clinical information into clear product requirements and compelling value propositions.
In this role, you will help shape the next generation of our medical software solutions and work at the intersection of customers, market, technology, and development. You will take on strategic responsibilities in upstream product management while closely collaborating on the execution and development of our digital products. o Analyze user requirements, clinical and fitness workflows, market trends, and competitive landscapes. * Drive software development from concept to market * Strong understanding of agile development practices and experience working with software engineering and UX/UI teams. * Ability to convert complex technical and clinical information into clear product requirements and compelling value propositions.
Research Data Infrastructure Engineer
Research Data Infrastructure Engineer
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
Contribute to interdisciplinary efforts, bridging cutting-edge research with clinical applications * Unleash your full potential: targeted offers for your personal development to further develop your talents
Contribute to interdisciplinary efforts, bridging cutting-edge research with clinical applications * Unleash your full potential: targeted offers for your personal development to further develop your talents
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