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10 Treffer für Clinical Research Jobs in Heidenheim An Der Brenz im Umkreis von 30 km
Noch nichts dabei? Es gibt 10 weitere Jobs, die zu deiner Suche passen könnten
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Als Clinical Trial Manager (m/w/d) bringst du dein Know-how und deine Expertise ein. * Verantwortung für die Clinical Trial Supply in Zusammenarbeit mit globalen * Mehrjährige Berufserfahrung im Bereich Clinical Operations/Clinical Trial Management wünschenswert
Als Clinical Trial Manager (m/w/d) bringst du dein Know-how und deine Expertise ein. * Verantwortung für die Clinical Trial Supply in Zusammenarbeit mit globalen * Mehrjährige Berufserfahrung im Bereich Clinical Operations/Clinical Trial Management wünschenswert
NEU
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Digital Optometry Product Lead (f/m/x) @ Carl Zeiss Extended Reality (XRX)
Digital Optometry Product Lead (f/m/x) @ Carl Zeiss Extended Reality (XRX)
ZEISS
Aalen (Baden-Württemberg)
Teilweise Home-Office
Define clinical and technical requirements for online eye testing and centration * Practical optometry/clinical vision science experience, in-store optical retail experience * Optometry / clinical vision science: Deep understanding of eye anatomy, refraction, centration principals and clinical standards as well as practical experience as optometrist or optician. * Technical product development: Experience collaborating with and to translate clinical requirements into digital solutions. * Communication: Effectively communicate clinical and technical concepts across diverse teams and stakeholders
Define clinical and technical requirements for online eye testing and centration * Practical optometry/clinical vision science experience, in-store optical retail experience * Optometry / clinical vision science: Deep understanding of eye anatomy, refraction, centration principals and clinical standards as well as practical experience as optometrist or optician. * Technical product development: Experience collaborating with and to translate clinical requirements into digital solutions. * Communication: Effectively communicate clinical and technical concepts across diverse teams and stakeholders
Application Specialist Integrated Photonics in Semiconductor Manufacturing (m/f/x)
Application Specialist Integrated Photonics in Semiconductor Manufacturing (m/f/x)
ZEISS
Oberkochen (Baden-Württemberg)
Utilize diverse information sources, including industry collaborations, internal research teams and institutions to stay at the forefront of photonic advancements. * Collaborate closely with customers, research institutions, and internal and cross-business-unit R&D departments to align development with industry needs. * Important: Extensive professional network in the photonics and semiconductor industry, including research institutions and chip manufacturers. * Strong analytical skills and the ability to translate application knowledge and cutting-edge research into practical equipment solutions.
Utilize diverse information sources, including industry collaborations, internal research teams and institutions to stay at the forefront of photonic advancements. * Collaborate closely with customers, research institutions, and internal and cross-business-unit R&D departments to align development with industry needs. * Important: Extensive professional network in the photonics and semiconductor industry, including research institutions and chip manufacturers. * Strong analytical skills and the ability to translate application knowledge and cutting-edge research into practical equipment solutions.
As a 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 own our applicative and clinical understanding of spine microsurgery procedures, you observe current trends and developments in clinics and industry * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in spine 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 establish and maintain a close customer interface in spine clinical environment * At least 5 years (8 years preferred) of professional experience in the medical industry or in a clinical environment
As a 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 own our applicative and clinical understanding of spine microsurgery procedures, you observe current trends and developments in clinics and industry * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in spine 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 establish and maintain a close customer interface in spine clinical environment * At least 5 years (8 years preferred) of professional experience in the medical industry or in a clinical environment
University Degree in Business Administration, Management, Project Management, Engineering or a related field or clinical background within Eye Care e.g. Optometrist
University Degree in Business Administration, Management, Project Management, Engineering or a related field or clinical background within Eye Care e.g. Optometrist
Solid understanding of product development lifecycles, from research and concept through design, industrialization, and market introduction
Solid understanding of product development lifecycles, from research and concept through design, industrialization, and market introduction
Market Research: Monitor industry trends, activities, and regulatory changes to enlarge and manage the IP portfolio as well as to mitigate risks.
Market Research: Monitor industry trends, activities, and regulatory changes to enlarge and manage the IP portfolio as well as to mitigate risks.
At ZEISS Corporate Research and Technology, we push the boundaries of what is possible to solve real world problems in this field.
At ZEISS Corporate Research and Technology, we push the boundaries of what is possible to solve real world problems in this field.
Capability Enhancement: Research and evaluate new tools, techniques, and data sources to enhance overall threat intelligence capabilities.
Capability Enhancement: Research and evaluate new tools, techniques, and data sources to enhance overall threat intelligence capabilities.
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Ausbildung und Praktikum
Ausbildung und Praktikum
JRS Pharma GmbH & Co. KG
Marienstraße 20, 89518 Heidenheim an der Brenz, Deutschland
Schnelle Bewerbung
Marketing Research
Marketing Research
34 passende Jobs liegen außerhalb deiner Region
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Werkstudenten (m/w/d) Research Systems * Du arbeitest im Bereich Research bei der Erstellung und Erprobung von neuen Konzepten und Produkten mit.
Werkstudenten (m/w/d) Research Systems * Du arbeitest im Bereich Research bei der Erstellung und Erprobung von neuen Konzepten und Produkten mit.
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Pflichtpraktikum als Market Research Consultant (quantitativ oder qualitativ)
Pflichtpraktikum als Market Research Consultant (quantitativ oder qualitativ)
advise research gmbh
Ulm
Teilweise Home-Office
Schnelle Bewerbung
advise research gmbh
advise research gmbh
Schnelle Bewerbung
advise research gmbh * Du wirkst bei Akquise-Aktionen mit und hilfst unsere Tools im Bereich Social Media & Market Research zu vermarkten
advise research gmbh * Du wirkst bei Akquise-Aktionen mit und hilfst unsere Tools im Bereich Social Media & Market Research zu vermarkten
Pflichtpraktikum als Data Analyst eines Marktforschung-Instituts
Pflichtpraktikum als Data Analyst eines Marktforschung-Instituts
advise research gmbh
Ulm
Teilweise Home-Office
Schnelle Bewerbung
advise research gmbh
advise research gmbh
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Organisation von Open Innovation Workshops mit externen Partnern (Rohstoffindustrie, Hochschulen, Forschungsinstituten sowie Kunden) und internen Teams, um Grundlagen- und Technologieentwicklung frühzeitig zu identifizieren und konkrete Projekte für unser Technology & Research Lab zu definieren
Organisation von Open Innovation Workshops mit externen Partnern (Rohstoffindustrie, Hochschulen, Forschungsinstituten sowie Kunden) und internen Teams, um Grundlagen- und Technologieentwicklung frühzeitig zu identifizieren und konkrete Projekte für unser Technology & Research Lab zu definieren
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Opportunity: We are seeking a highly motivated Senior Research Engineer to join our team in designing, developing, and maintaining the next generation AI-powered Natural Language Understanding (NLU) systems for the automotive and mobility markets.
Opportunity: We are seeking a highly motivated Senior Research Engineer to join our team in designing, developing, and maintaining the next generation AI-powered Natural Language Understanding (NLU) systems for the automotive and mobility markets.
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Senior Clinical Trial Project Manager MD (m/f/d) 80–100%
Senior Clinical Trial Project Manager MD (m/f/d) 80–100%
regenold GmbH
bundesweit, Home-Office
Teilweise Home-Office
In this client-facing consulting role, as part of the you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors. * Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field * Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications * Managing clinical investigations end to end, from study planning to close-out * 6+ years of hands-on experience in managing clinical trials with solid experience in clinical investigations * Proven track record in such as (Senior) Clinical Project Manager / Lead, ideally across different settings (Pharma, CRO) * Profound knowledge of GCP and the clinical regulatory environment
In this client-facing consulting role, as part of the you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors. * Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field * Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications * Managing clinical investigations end to end, from study planning to close-out * 6+ years of hands-on experience in managing clinical trials with solid experience in clinical investigations * Proven track record in such as (Senior) Clinical Project Manager / Lead, ideally across different settings (Pharma, CRO) * Profound knowledge of GCP and the clinical regulatory environment
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Field Clinical Specialist TMTT – Baden‑Württemberg
Field Clinical Specialist TMTT – Baden‑Württemberg
Edwards Lifesciences GmbH
Baden-Württemberg
Teilweise Home-Office
Schnelle Bewerbung
Develops clinical education materials in connection with clinical investigations. Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clinical investigation. • Provide feedback to improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP • Perform routine reviews on clinical support activities, changes in the market and assigned accounts, as well as, competitive activity with cross-functional teams (e.g., sales) Bachelor's Degree in in related field Training experience in clinical / technical environment Required - Other: 3 year experience of previous related medical device and/or clinical experience Required
Develops clinical education materials in connection with clinical investigations. Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clinical investigation. • Provide feedback to improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP • Perform routine reviews on clinical support activities, changes in the market and assigned accounts, as well as, competitive activity with cross-functional teams (e.g., sales) Bachelor's Degree in in related field Training experience in clinical / technical environment Required - Other: 3 year experience of previous related medical device and/or clinical experience Required
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Close collaboration with Product Management, Research & Development, and an international Clinical Application Specialist network * Representation of clinical practice within product development projects * Support of clinical validation and testing activities * Structured collection and provision of clinical feedback on existing products * Building and maintaining a professional clinical network in emergency and respiratory care * Completed clinical training as a paramedic (preferred), ideally complemented by qualification as a critical care nurse or a comparable advanced certification
Close collaboration with Product Management, Research & Development, and an international Clinical Application Specialist network * Representation of clinical practice within product development projects * Support of clinical validation and testing activities * Structured collection and provision of clinical feedback on existing products * Building and maintaining a professional clinical network in emergency and respiratory care * Completed clinical training as a paramedic (preferred), ideally complemented by qualification as a critical care nurse or a comparable advanced certification
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SAP Consultant (m/w/d) Research & Development Chemie / Pharma
SAP Consultant (m/w/d) Research & Development Chemie / Pharma
SI PRO GmbH Gesellschaft für Systemintegration und Geschäftsprozeßgestaltung
Mannheim, Berlin, Hamburg, München, bundesweit (Home-Office)
Teilweise Home-Office
Als Consultant (w/m/d) im Bereich Research & Development Chemie / Pharma / SAP unterstützt du führende Unternehmen aus der Prozessindustrie im Rahmen von multidisziplinären Beratungsprojekten.
Als Consultant (w/m/d) im Bereich Research & Development Chemie / Pharma / SAP unterstützt du führende Unternehmen aus der Prozessindustrie im Rahmen von multidisziplinären Beratungsprojekten.
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Clinical Support Specialist / Anwendungsexperte (m/w/d)
Clinical Support Specialist / Anwendungsexperte (m/w/d)
ACANDIS GmbH
Norddeutschland, Ostdeutschland, Süddeutschland, Westdeutschland
Schnelle Bewerbung
Zum nächstmöglichen Zeitpunkt suchen wir einen Clinical Support Specialist / Anwendungsexperte (m/w/d) Als Clinical Support Specialist Deutschland arbeiten Sie an der Schnittstelle zwischen unseren Technologien und den Ärzten in den Kliniken. * Enger Austausch innerhalb des Clinical Support Teams sowie mit den Unternehmensbereichen Entwicklung, Klinische Forschung und Medical Affairs
Zum nächstmöglichen Zeitpunkt suchen wir einen Clinical Support Specialist / Anwendungsexperte (m/w/d) Als Clinical Support Specialist Deutschland arbeiten Sie an der Schnittstelle zwischen unseren Technologien und den Ärzten in den Kliniken. * Enger Austausch innerhalb des Clinical Support Teams sowie mit den Unternehmensbereichen Entwicklung, Klinische Forschung und Medical Affairs
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Associate Director Regulatory Affairs – CMC Lead*
Associate Director Regulatory Affairs – CMC Lead*
Immatics Biotechnologies GmbH
Tübingen, München, Home-Office
Teilweise Home-Office
In this role, you will provide strategic CMC regulatory leadership for innovative oncology biopharmaceutical and ATMP programs across clinical development phases. You will independently lead EU CMC regulatory strategy and execution for assigned programs across early and late-stage clinical development. * Own EU CMC regulatory strategy for assigned clinical-stage programs (phase I–III). * Lead preparation and coordination of CMC/ GMP documentation for submission of initial clinical trial applications as well as Substantial Modifications. * Strong experience preparing CMC-related information/ documents for clinical trial applications and supporting Health Authority interactions.
In this role, you will provide strategic CMC regulatory leadership for innovative oncology biopharmaceutical and ATMP programs across clinical development phases. You will independently lead EU CMC regulatory strategy and execution for assigned programs across early and late-stage clinical development. * Own EU CMC regulatory strategy for assigned clinical-stage programs (phase I–III). * Lead preparation and coordination of CMC/ GMP documentation for submission of initial clinical trial applications as well as Substantial Modifications. * Strong experience preparing CMC-related information/ documents for clinical trial applications and supporting Health Authority interactions.
Schnelle Bewerbung
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. * Strong understanding of clinical workflows, healthcare economics, and value-based selling in medical devices. * Advanced relationship-building and stakeholder management skills; ability to influence senior (non-)clinical and .
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. * Strong understanding of clinical workflows, healthcare economics, and value-based selling in medical devices. * Advanced relationship-building and stakeholder management skills; ability to influence senior (non-)clinical and .
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Schnelle Bewerbung
Du unterstützt beim User Research und Usability-Testing, indem du Interviews führst, Umfragen durchführst und Prototyp-Tests begleitest * Grundkenntnisse in User Research und Usability-Testing sind ein Plus
Du unterstützt beim User Research und Usability-Testing, indem du Interviews führst, Umfragen durchführst und Prototyp-Tests begleitest * Grundkenntnisse in User Research und Usability-Testing sind ein Plus
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Weiterbildung: umfangreiche fachliche und methodische Trainings inkl. Zertifizierungen sowie vielfältige Entwicklungsperspektiven innerhalb des Unternehmens, monatlicher Research Day und ein großzügiges Schulungsbudget von bis zu 10 Tagen im Jahr
Weiterbildung: umfangreiche fachliche und methodische Trainings inkl. Zertifizierungen sowie vielfältige Entwicklungsperspektiven innerhalb des Unternehmens, monatlicher Research Day und ein großzügiges Schulungsbudget von bis zu 10 Tagen im Jahr