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52.565 Treffer für Clinical Data Management Jobs
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Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung von Projekten entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. INCONSULT ist eine spezialisierte Management- und IT-Beratung mit Fokus auf Prozessberatung und digitale Transformation in der Life-Science-Industrie. Für den weiteren Ausbau der Prozessdomäne Clinical suchen wir zum nächstmöglichen Zeitpunkt einen Senior Consultant Clinical Operations (m/w/d) mit dem Schwerpunkt Patient Centricity. * Methodenkompetenz im Consulting und Projektmanagement
Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung von Projekten entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. INCONSULT ist eine spezialisierte Management- und IT-Beratung mit Fokus auf Prozessberatung und digitale Transformation in der Life-Science-Industrie. Für den weiteren Ausbau der Prozessdomäne Clinical suchen wir zum nächstmöglichen Zeitpunkt einen Senior Consultant Clinical Operations (m/w/d) mit dem Schwerpunkt Patient Centricity. * Methodenkompetenz im Consulting und Projektmanagement
Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. INCONSULT ist eine spezialisierte Management- und IT-Beratung mit Fokus auf Prozessberatung und digitaler Transformation in der Life-Science-Industrie. * Strategische und strukturelle Beratung des Top-Managements nationaler und internationaler Kunden bei der Umsetzung ihrer digitalen Transformation * Enge Zusammenarbeit mit angrenzenden Disziplinen (z.B. Clinical) * Erfahrung in der Kundenführung auf Top-Management-Ebene * Methodenkompetenz in Projekt-, Change- und Innovationsmanagement
Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. INCONSULT ist eine spezialisierte Management- und IT-Beratung mit Fokus auf Prozessberatung und digitaler Transformation in der Life-Science-Industrie. * Strategische und strukturelle Beratung des Top-Managements nationaler und internationaler Kunden bei der Umsetzung ihrer digitalen Transformation * Enge Zusammenarbeit mit angrenzenden Disziplinen (z.B. Clinical) * Erfahrung in der Kundenführung auf Top-Management-Ebene * Methodenkompetenz in Projekt-, Change- und Innovationsmanagement
Noch nichts dabei? Es gibt 52563 weitere Jobs, die zu deiner Suche passen könnten
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Clinical Scientific Program Lead (all genders)
Clinical Scientific Program Lead (all genders)
medac Gesellschaft für klinische Spezialpräparate mbH
Wedel bei Hamburg
Teilweise Home-Office
Schnelle Bewerbung
Lead global clinical development programs across Phase I–III trials, overseeing multiple studies and ensuring high-quality execution, data integrity, and timely delivery - At our location in near Hamburg, we are looking for a clinical scientific program lead (all genders). * Clinical science program lead with extensive expe rience in global clinical develop ment across Phase I–IV, with a strong focus on auto immune diseases, immunology, and inno vative therapies * Proven track record in designing smart, integrated clinical development programs, evaluating new assets through due diligence, and advancing lifecycle strategies, including indication extensions and territory expansions * Experienced in leading cross-functional teams, delivering high-quality data packages, and driving successful interacctions with regulatory authorities (EMA / FDA)
Lead global clinical development programs across Phase I–III trials, overseeing multiple studies and ensuring high-quality execution, data integrity, and timely delivery - At our location in near Hamburg, we are looking for a clinical scientific program lead (all genders). * Clinical science program lead with extensive expe rience in global clinical develop ment across Phase I–IV, with a strong focus on auto immune diseases, immunology, and inno vative therapies * Proven track record in designing smart, integrated clinical development programs, evaluating new assets through due diligence, and advancing lifecycle strategies, including indication extensions and territory expansions * Experienced in leading cross-functional teams, delivering high-quality data packages, and driving successful interacctions with regulatory authorities (EMA / FDA)
Medical Expert – Clinical Science (all genders)
Medical Expert – Clinical Science (all genders)
medac Gesellschaft für klinische Spezialpräparate mbH
Wedel bei Hamburg
Teilweise Home-Office
Schnelle Bewerbung
You are a hands-on Medical Expert responsible for executing clinical-scientific activities across the product lifecycle, focussed on the development of high-quality regulatory documentation (CTD) and support of global submissions and lifecycle management. You act as a cross-functional clinical partner, translating clinical data into consistent scientific messaging and supporting decision-making across clinical science. * Author, review and lead high-quality clinical and regulatory documents (CTD), including Clinical Overview & Clinical Summary, Clinical Expert Statements, Risk Management Plans (RMPs), SmPC, CCDS, PIL, PSURs / DSURs and other lifecycle documents - At our location in Wedel near Hamburg, we are looking for a Medical Expert – Clinical Science (all genders). You lead and evaluate medac's Managed Access Programs (MAP) and Named Patient Use (NPU) requests from a clinical and ...
You are a hands-on Medical Expert responsible for executing clinical-scientific activities across the product lifecycle, focussed on the development of high-quality regulatory documentation (CTD) and support of global submissions and lifecycle management. You act as a cross-functional clinical partner, translating clinical data into consistent scientific messaging and supporting decision-making across clinical science. * Author, review and lead high-quality clinical and regulatory documents (CTD), including Clinical Overview & Clinical Summary, Clinical Expert Statements, Risk Management Plans (RMPs), SmPC, CCDS, PIL, PSURs / DSURs and other lifecycle documents - At our location in Wedel near Hamburg, we are looking for a Medical Expert – Clinical Science (all genders). You lead and evaluate medac's Managed Access Programs (MAP) and Named Patient Use (NPU) requests from a clinical and ...
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Schnelle Bewerbung
The successful candidate should not only understand clinical pharmacology, DMPK, PopPK, PBPK, PK/PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. • Interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into pragmatic, regulatorily defensible development decisions. • Advise on nonclinical , ADME, pharmacology, toxicology, and translational data packages to ensure they support clinical and regulatory objectives. • Proven ability to interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into clear, pragmatic, and regulatorily defensible development recommendations. • Strong scientific writing, communication, and stakeholder-management skills, with the ability to explain complex ...
The successful candidate should not only understand clinical pharmacology, DMPK, PopPK, PBPK, PK/PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. • Interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into pragmatic, regulatorily defensible development decisions. • Advise on nonclinical , ADME, pharmacology, toxicology, and translational data packages to ensure they support clinical and regulatory objectives. • Proven ability to interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into clear, pragmatic, and regulatorily defensible development recommendations. • Strong scientific writing, communication, and stakeholder-management skills, with the ability to explain complex ...
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Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
AstraZeneca
Bayern
Teilweise Home-Office
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
AstraZeneca
Hamburg
Teilweise Home-Office
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
In unserem Bereich Site Management & Monitoring findet mit der Durchführung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese möglichst schnell und umfangreich erprobt als moderne Therapieoptionen für Patient:innen verfügbar zu machen. Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst) * Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring * Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports
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Clinical Research Associate / Klinischer Monitor (m/w/d)
Clinical Research Associate / Klinischer Monitor (m/w/d)
IGES Institut GmbH
Berlin
Teilweise Home-Office
Schnelle Bewerbung
Wir forschen im Auftrag unserer Kunden darüber hinaus auch zu den Themen Inanspruchnahme, Medical Need, Patientenpräferenzen und Clinical Pathways. Zur Verstärkung unseres Teams in Berlin suchen wir zum nächstmöglichen Zeitpunkt einen Clinical Research Associate / Klinischen Monitor (m/w/d). * Management und/oder Unterstützung von Studienzentren * Sicherstellung der Validität der Studiendaten und Erstellen von Data Queries
Wir forschen im Auftrag unserer Kunden darüber hinaus auch zu den Themen Inanspruchnahme, Medical Need, Patientenpräferenzen und Clinical Pathways. Zur Verstärkung unseres Teams in Berlin suchen wir zum nächstmöglichen Zeitpunkt einen Clinical Research Associate / Klinischen Monitor (m/w/d). * Management und/oder Unterstützung von Studienzentren * Sicherstellung der Validität der Studiendaten und Erstellen von Data Queries
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Schnelle Bewerbung
Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders * Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out * Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * 7–10+ years of experience in clinical research, including clinical project management * Minimum of 5 years of hands-on experience in clinical project management To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Oversee safety reporting activities, management of protocol deviations, and ensure inspection readiness
Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders * Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out * Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * 7–10+ years of experience in clinical research, including clinical project management * Minimum of 5 years of hands-on experience in clinical project management To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Oversee safety reporting activities, management of protocol deviations, and ensure inspection readiness
Senior Scientist (m/f/d), Computational Pathology Biomarker Lead (BioPharmaceuticals)
Senior Scientist (m/f/d), Computational Pathology Biomarker Lead (BioPharmaceuticals)
AstraZeneca
München
In this role, you will collaborate with cross-functional teams to generate data-driven insights that inform clinical decisions across therapeutic areas such as cardiovascular, renal, metabolic, and respiratory diseases. Work at the interface of biology, data science, and AI to generate actionable insights throughout drug development - from target validation to clinical implementation. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. AstraZeneca's Enterprise AI organization is building the future of drug development by connecting data, technology, and expertise to accelerate breakthroughs across our portfolio. Within Computational Pathology and Biomarkers, we develop AI-powered solutions to advance patient selection, biomarker development, and clinical decision-making at scale.
In this role, you will collaborate with cross-functional teams to generate data-driven insights that inform clinical decisions across therapeutic areas such as cardiovascular, renal, metabolic, and respiratory diseases. Work at the interface of biology, data science, and AI to generate actionable insights throughout drug development - from target validation to clinical implementation. At Computational Pathology Munich (CPM), we make a significant contribution to high-performance, data-driven research and development. AstraZeneca's Enterprise AI organization is building the future of drug development by connecting data, technology, and expertise to accelerate breakthroughs across our portfolio. Within Computational Pathology and Biomarkers, we develop AI-powered solutions to advance patient selection, biomarker development, and clinical decision-making at scale.
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Schnelle Bewerbung
Statistical analysis and evaluation of clinical data (hands-on) * Management, support and coordination of in the preparation and maintenance of clinical evaluations * Deep knowledge of disease state, clinical information, and product data for the business - A leading company in several diagnostics niche markets including Immunochemistry, HPLC based diabetes and thalassemia screening and Molecular Biology has demonstrated technological leadership through an in-depth understanding of the ever-growing clinical demand for faster and more precise diagnosis of several life-threatening pathologies (e.g., tumour, cardiac, diabetes etc.). The role acts as a central interface between scientific/clinical, QARA, Sales, Marketing and Strategy. You provide high-quality scientific and application support to internal and external customers, delivering evidence-based expertise across Scientific ...
Statistical analysis and evaluation of clinical data (hands-on) * Management, support and coordination of in the preparation and maintenance of clinical evaluations * Deep knowledge of disease state, clinical information, and product data for the business - A leading company in several diagnostics niche markets including Immunochemistry, HPLC based diabetes and thalassemia screening and Molecular Biology has demonstrated technological leadership through an in-depth understanding of the ever-growing clinical demand for faster and more precise diagnosis of several life-threatening pathologies (e.g., tumour, cardiac, diabetes etc.). The role acts as a central interface between scientific/clinical, QARA, Sales, Marketing and Strategy. You provide high-quality scientific and application support to internal and external customers, delivering evidence-based expertise across Scientific ...
In this role, you will collaborate with multidisciplinary teams to data-driven approaches that generate impactful insights and improve clinical outcomes. Working at the intersection of data, AI innovation, and tumor biology, you will collaborate in cross-functional teams to develop and implement computational pathology solutions from early discovery through clinical validation, generating high-quality translational insights that support critical decisions and advance precision medicine. * Integrate tissue, imaging, genomics, and clinical data to inform project strategy and clinical decision-making. * Contribute to project quality through data review, reporting, presentations, publications, and input into clinical and regulatory documents. * Proven ability to generate insights from complex, multi-modal datasets, including tissue, imaging, genomic, and clinical data.
In this role, you will collaborate with multidisciplinary teams to data-driven approaches that generate impactful insights and improve clinical outcomes. Working at the intersection of data, AI innovation, and tumor biology, you will collaborate in cross-functional teams to develop and implement computational pathology solutions from early discovery through clinical validation, generating high-quality translational insights that support critical decisions and advance precision medicine. * Integrate tissue, imaging, genomics, and clinical data to inform project strategy and clinical decision-making. * Contribute to project quality through data review, reporting, presentations, publications, and input into clinical and regulatory documents. * Proven ability to generate insights from complex, multi-modal datasets, including tissue, imaging, genomic, and clinical data.
Schnelle Bewerbung
Advanced relationship-building and stakeholder management skills; ability to influence senior (non-)clinical and . The focus of this role will be to drive the strategic account management (SAM) program in Germany, ensuring alignment with locally defined country xBU SHD objectives and focusing on achieving sustainable growth within the most strategic hospital accounts. * Build deep and trustful relationships with key decision-makers and influencers (clinical, economic, administrative) by demonstrating consistency and accountability. * Integrate country business performance and market insights (, reimbursement, clinical trends) to inform country portfolio and commercial strategies. * Typically 7+ years of proven sales, key account management and/or marketing experience, with 3–5 years+ in medical device or healthcare sector. * Strong understanding of clinical workflows, healthcare ...
Advanced relationship-building and stakeholder management skills; ability to influence senior (non-)clinical and . The focus of this role will be to drive the strategic account management (SAM) program in Germany, ensuring alignment with locally defined country xBU SHD objectives and focusing on achieving sustainable growth within the most strategic hospital accounts. * Build deep and trustful relationships with key decision-makers and influencers (clinical, economic, administrative) by demonstrating consistency and accountability. * Integrate country business performance and market insights (, reimbursement, clinical trends) to inform country portfolio and commercial strategies. * Typically 7+ years of proven sales, key account management and/or marketing experience, with 3–5 years+ in medical device or healthcare sector. * Strong understanding of clinical workflows, healthcare ...
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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
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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Country Marketing Manager, TMTT Germany
Country Marketing Manager, TMTT Germany
Edwards Lifesciences GmbH
Bayern, europaweit
Teilweise Home-Office
Schnelle Bewerbung
Understand customer and commercial teams' needs through regular field presence, localize marketing assets, and develop thorough knowledge of therapy, clinical data and competitive landscape * Lead the development and continuous evolution of the German TMTT marketing strategy, ensuring alignment with the European vision while tailoring approaches to local market dynamics, regulatory frameworks, and unmet clinical needs. * Support customer segmentation and KOL management * Partner closely with Medical Affairs, Clinical, and Commercial on segmentation, KOL engagement pathways, and strategic partnerships within the German cardiology community. * Proven successful project management skills * Excellent written and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
Understand customer and commercial teams' needs through regular field presence, localize marketing assets, and develop thorough knowledge of therapy, clinical data and competitive landscape * Lead the development and continuous evolution of the German TMTT marketing strategy, ensuring alignment with the European vision while tailoring approaches to local market dynamics, regulatory frameworks, and unmet clinical needs. * Support customer segmentation and KOL management * Partner closely with Medical Affairs, Clinical, and Commercial on segmentation, KOL engagement pathways, and strategic partnerships within the German cardiology community. * Proven successful project management skills * Excellent written and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
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Schnelle Bewerbung
Leverage strong scientific understanding to interpret preclinical and clinical data, support opportunity valuation, and strengthen negotiation positions with evidence-based insights. This is an opportunity to operate at the interface of science and business, translating complex data and strategic intent into high-quality agreements that shape Dr. Falk's development pipeline and partnerships. * Monitor contractual obligations, milestones, and governance processes; support renewals, amendments, and lifecycle management of agreements. * Strong scientific curiosity and understanding are essential; enabling you to critically evaluate assets and actively contribute to negotiations grounded in data and mechanism-based reasoning.
Leverage strong scientific understanding to interpret preclinical and clinical data, support opportunity valuation, and strengthen negotiation positions with evidence-based insights. This is an opportunity to operate at the interface of science and business, translating complex data and strategic intent into high-quality agreements that shape Dr. Falk's development pipeline and partnerships. * Monitor contractual obligations, milestones, and governance processes; support renewals, amendments, and lifecycle management of agreements. * Strong scientific curiosity and understanding are essential; enabling you to critically evaluate assets and actively contribute to negotiations grounded in data and mechanism-based reasoning.
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2–5 years of hands-on experience with Microsoft Dynamics 365 Finance & Operations (D365 F&O), preferably in Project Management and Accounting, Service Management, Project Operations, or related modules * Experience using SQL to analyze data, validate business rules, and support data-driven decision making - Our company fosters a culture where employees are encouraged to learn and innovate, and to enable and enhance clinical co-operation and processes while making a meaningful difference for millions of people around the world.
2–5 years of hands-on experience with Microsoft Dynamics 365 Finance & Operations (D365 F&O), preferably in Project Management and Accounting, Service Management, Project Operations, or related modules * Experience using SQL to analyze data, validate business rules, and support data-driven decision making - Our company fosters a culture where employees are encouraged to learn and innovate, and to enable and enhance clinical co-operation and processes while making a meaningful difference for millions of people around the world.
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Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture - The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. * Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS). * US: 3 years of experience in the pharmaceutical / biotechnology / CRO industry, 2 year of clinical monitoring experience with 1 year of management experience - The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, ...
Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture - The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. * Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS). * US: 3 years of experience in the pharmaceutical / biotechnology / CRO industry, 2 year of clinical monitoring experience with 1 year of management experience - The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, ...
Define user stories, acceptance criteria, and product requirements based on clinical workflows and user needs * Clinical decision support and AI * Real-time data integration & monitoring * Alternatively: significant clinical experience (e.g., ICU nurse, anesthesiology support) with strong IT affinity * 2–5 years in Product Management, Product Ownership, or similar roles in software development * 5–10 years in clinical environments (ICU, ER, anesthesia) with exposure to digital systems * Strong stakeholder management across international environments - Our company fosters a culture where employees are encouraged to learn and innovate, and to enable and enhance clinical co-operation and processes while making a meaningful difference for millions of people around the world.
Define user stories, acceptance criteria, and product requirements based on clinical workflows and user needs * Clinical decision support and AI * Real-time data integration & monitoring * Alternatively: significant clinical experience (e.g., ICU nurse, anesthesiology support) with strong IT affinity * 2–5 years in Product Management, Product Ownership, or similar roles in software development * 5–10 years in clinical environments (ICU, ER, anesthesia) with exposure to digital systems * Strong stakeholder management across international environments - Our company fosters a culture where employees are encouraged to learn and innovate, and to enable and enhance clinical co-operation and processes while making a meaningful difference for millions of people around the world.
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Schnelle Bewerbung
Project Management (approx. 40%): own and drive the delivery of clinical customer projects and ensure internal execution against external commitments * Act as the internal of clinical projects by pushing priorities, timelines, and decisions across product, data, and medical teams * Cross-functional influence: You work at the center of product, data, medical, and customer teams and translate clinical realities into execution and product improvements * 3+ years experience in clinical operations, healthcare project management, customer success, or similar roles - Synagen builds specialized AI agents for healthcare and oncology, designed to support complex clinical decisions and biomedical workflows with actionable, high-precision outputs. We combine modern AI with clinical expertise to create software that integrates into real provider environments and delivers value in practice.
Project Management (approx. 40%): own and drive the delivery of clinical customer projects and ensure internal execution against external commitments * Act as the internal of clinical projects by pushing priorities, timelines, and decisions across product, data, and medical teams * Cross-functional influence: You work at the center of product, data, medical, and customer teams and translate clinical realities into execution and product improvements * 3+ years experience in clinical operations, healthcare project management, customer success, or similar roles - Synagen builds specialized AI agents for healthcare and oncology, designed to support complex clinical decisions and biomedical workflows with actionable, high-precision outputs. We combine modern AI with clinical expertise to create software that integrates into real provider environments and delivers value in practice.
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Your code will support clinical researchers working with real patient data at scale. * Design with security at the core — shaping authorization concepts and data protection architecture from the ground up, including the documentation that supports review and sign-off by our clinical partners. By linking technology and research, we make health data available to research in a comprehensive, digital and secure way. Our interdisciplinary team in Potsdam, Berlin and Singapore brings together experts from fields such as product development, digital engineering, data security and science. As a nonprofit supported by the Hasso Plattner Foundation, we build scalable research infrastructures — supporting international standards such as FHIR and OMOP — and collaborate with some of the world's leading clinical institutions. * Work closely with , QA, and product management as part of an ...
Your code will support clinical researchers working with real patient data at scale. * Design with security at the core — shaping authorization concepts and data protection architecture from the ground up, including the documentation that supports review and sign-off by our clinical partners. By linking technology and research, we make health data available to research in a comprehensive, digital and secure way. Our interdisciplinary team in Potsdam, Berlin and Singapore brings together experts from fields such as product development, digital engineering, data security and science. As a nonprofit supported by the Hasso Plattner Foundation, we build scalable research infrastructures — supporting international standards such as FHIR and OMOP — and collaborate with some of the world's leading clinical institutions. * Work closely with , QA, and product management as part of an ...
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Senior Sales Manager – Marketing Solutions (Life Sciences) (m/w/d)
Senior Sales Manager – Marketing Solutions (Life Sciences) (m/w/d)
ResearchGate GmbH
Berlin
Teilweise Home-Office
The partnerships you build will bring vital tools, clinical data, and breakthrough technologies directly to the minds actively solving humanity's most complex medical and scientific challenges. * Collaborate for Campaign Success: Partner closely with Account Management and Ad Ops to ensure ad campaigns perform flawlessly against client KPIs, securing renewals and long-term retention.
The partnerships you build will bring vital tools, clinical data, and breakthrough technologies directly to the minds actively solving humanity's most complex medical and scientific challenges. * Collaborate for Campaign Success: Partner closely with Account Management and Ad Ops to ensure ad campaigns perform flawlessly against client KPIs, securing renewals and long-term retention.
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Medical imaging AI is advancing rapidly, however, research effort is often shaped by data availability rather than clinical need. Through a large-scale crowdsourcing campaign, clinicians, and researchers worldwide will contribute challenging clinical questions and medical imaging data. This is a technically demanding role with real architectural ownership: you will shape how clinical data flows into the project, how it is stored and protected, and how AI models are evaluated against the benchmark, and you will be hands-on in implementing these systems alongside a software developer. MEDAL (Medical Imaging AGI's Last Exam is an international initiative funded by the Carl-Zeiss-Stiftung that aims to change this by building a globally relevant benchmark grounded in real clinical priorities. An international, multidisciplinary expert panel will curate the benchmark to ensure ...
Medical imaging AI is advancing rapidly, however, research effort is often shaped by data availability rather than clinical need. Through a large-scale crowdsourcing campaign, clinicians, and researchers worldwide will contribute challenging clinical questions and medical imaging data. This is a technically demanding role with real architectural ownership: you will shape how clinical data flows into the project, how it is stored and protected, and how AI models are evaluated against the benchmark, and you will be hands-on in implementing these systems alongside a software developer. MEDAL (Medical Imaging AGI's Last Exam is an international initiative funded by the Carl-Zeiss-Stiftung that aims to change this by building a globally relevant benchmark grounded in real clinical priorities. An international, multidisciplinary expert panel will curate the benchmark to ensure ...
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Release Engineer / Technical Lead, Software & Electronics (m/w/d)
Release Engineer / Technical Lead, Software & Electronics (m/w/d)
Ambu Innovation
Augsburg
Teilweise Home-Office
Ensuring compliance with relevant standards and regulations, such as IEC 62304, SaMD, ISO 14971, MDR / FDA requirements, and emerging AI-related guidance and standards (e.g. AI/ML lifecycle management, data management). * Understanding of AI-specific challenges such as data dependency, model performance, validation, change management, and lifecycle maintenance in regulated products. Would you like to take a leading role in bringing regulated AI solutions safely and efficiently into clinical use? In this role, you will be involved in all phases of the product lifecycle – from early concept and architectural decisions through development, verification, regulatory submission, market release, and sustained lifecycle management. You will combine deep technical understanding with a strong design control discipline, acting as the technical anchor between AI/ML developers, system engineers, quality, ...
Ensuring compliance with relevant standards and regulations, such as IEC 62304, SaMD, ISO 14971, MDR / FDA requirements, and emerging AI-related guidance and standards (e.g. AI/ML lifecycle management, data management). * Understanding of AI-specific challenges such as data dependency, model performance, validation, change management, and lifecycle maintenance in regulated products. Would you like to take a leading role in bringing regulated AI solutions safely and efficiently into clinical use? In this role, you will be involved in all phases of the product lifecycle – from early concept and architectural decisions through development, verification, regulatory submission, market release, and sustained lifecycle management. You will combine deep technical understanding with a strong design control discipline, acting as the technical anchor between AI/ML developers, system engineers, quality, ...
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Schnelle Bewerbung
The CSM works in close collaboration with Study Start-Up (SSU) manager, Clinical Study Administrator (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. * Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP). The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements. The CSM is responsible for ensuring that all requirements for site activation are in place for the agreed number of centers in clinical studies according to SOPs. * Quality and timeliness of study deliverables (site identification, feasibility, start up, ...
The CSM works in close collaboration with Study Start-Up (SSU) manager, Clinical Study Administrator (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. * Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP). The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements. The CSM is responsible for ensuring that all requirements for site activation are in place for the agreed number of centers in clinical studies according to SOPs. * Quality and timeliness of study deliverables (site identification, feasibility, start up, ...
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