Schnelle Bewerbung
1462
Erscheinungsdatum
Home-Office-Optionen
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Filter
SortierungRelevanz
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Stuttgart
- Düsseldorf
- Hannover
- Leipzig
- Dresden
- Nürnberg
- Essen
- Karlsruhe
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Ulm
- Heidelberg
- Walldorf, Baden-Württemberg
- Gilching
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Niederrhein
- Taunus
- Oberbayern
Home-Office-Optionen
Gehalt
Leg fest, wie viel du mindestens verdienen willst.
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Stuttgart
- Düsseldorf
- Hannover
- Leipzig
- Dresden
- Nürnberg
- Essen
- Karlsruhe
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Ulm
- Heidelberg
- Walldorf, Baden-Württemberg
- Gilching
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Niederrhein
- Taunus
- Oberbayern
4.288 Treffer für Clinical Development Jobs
Schnelle Bewerbung
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. * Provides medical risk assessment for activities related to clinical trials and development programs * A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required * Knowledge in clinical development in gastroenterology and/or hepatology is beneficial * Significant experience with clinical evaluation projects including the development of Clinical Trial Protocols, case report forms, Informed Consent Forms and Investigator Brochures.
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. * Provides medical risk assessment for activities related to clinical trials and development programs * A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required * Knowledge in clinical development in gastroenterology and/or hepatology is beneficial * Significant experience with clinical evaluation projects including the development of Clinical Trial Protocols, case report forms, Informed Consent Forms and Investigator Brochures.
){kind=logo}
Global Medical Scientific Writer - 70% part-time (m/f/d)
Global Medical Scientific Writer - 70% part-time (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
Working within and guiding cross-functional teams from clinical development to medical affairs in order to bring safe and effective medicines to patients - To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are a healthcare enthusiast who is capable of adeptly assimilating and interpreting clinical efficacy and safety data or other scientific content into a logical, scientifically balanced compelling medical narrative for the appropriate audience. * Planning, writing, reviewing and submitting manuscripts on clinical drug trials in humans for peer-reviewed journals and abstracts for scientific conferences
Working within and guiding cross-functional teams from clinical development to medical affairs in order to bring safe and effective medicines to patients - To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are a healthcare enthusiast who is capable of adeptly assimilating and interpreting clinical efficacy and safety data or other scientific content into a logical, scientifically balanced compelling medical narrative for the appropriate audience. * Planning, writing, reviewing and submitting manuscripts on clinical drug trials in humans for peer-reviewed journals and abstracts for scientific conferences
NEU
Development Program Lead Science & Innovation (m/f/d)
Development Program Lead Science & Innovation (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
Several years of experience in drug development (e.g., preclinical or clinical development in Phases I–III) and cross-functional program management - The Development Program Lead (DPL) is responsible for the strategic and operational management of a development program from the early stages through to approval. The DPL develops the cross-functional development strategy in collaboration with the Integrated (IDT), oversees its implementation across all functions, and serves as the central point of contact for the Steering Committee and external partners. The IDT consists of the following functions: Pre- & Early Clinical Research, Clinical Research, CMC Project Management, Global Safety, Global Medical, Global Commercial New Products, Global Market Access, Intellectual Property and Technical Operations. * When development programs are carried out in collaboration with external , the ...
Several years of experience in drug development (e.g., preclinical or clinical development in Phases I–III) and cross-functional program management - The Development Program Lead (DPL) is responsible for the strategic and operational management of a development program from the early stages through to approval. The DPL develops the cross-functional development strategy in collaboration with the Integrated (IDT), oversees its implementation across all functions, and serves as the central point of contact for the Steering Committee and external partners. The IDT consists of the following functions: Pre- & Early Clinical Research, Clinical Research, CMC Project Management, Global Safety, Global Medical, Global Commercial New Products, Global Market Access, Intellectual Property and Technical Operations. * When development programs are carried out in collaboration with external , the ...
Clinical Research - Head of Gastroenterology II (m/f/d)
Clinical Research - Head of Gastroenterology II (m/f/d)
Dr. Falk Pharma GmbH
Freiburg im Breisgau
Teilweise Home-Office
Schnelle Bewerbung
Serves as group lead (GL) for the company-sponsored clinical trials and development programs in the therapeutic area of functional gastrointestinal and gastrointestinal motility disorders. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials within this therapeutic area. * Review and approval of critical development documents (e.g., Clinical Trial Protocol, master ICF, Statistical Analysis Plan, Clinical Trial Protocol) * Support for the of Clinical Research in preparing and updating clinical development plans * Cross-functional support in the clinical assessment of research and/or study proposals, development offers, and Go/No-Go decisions in clinical development * A minimum of 5 years of clinical development research and clinical study project management, or related ...
Serves as group lead (GL) for the company-sponsored clinical trials and development programs in the therapeutic area of functional gastrointestinal and gastrointestinal motility disorders. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials within this therapeutic area. * Review and approval of critical development documents (e.g., Clinical Trial Protocol, master ICF, Statistical Analysis Plan, Clinical Trial Protocol) * Support for the of Clinical Research in preparing and updating clinical development plans * Cross-functional support in the clinical assessment of research and/or study proposals, development offers, and Go/No-Go decisions in clinical development * A minimum of 5 years of clinical development research and clinical study project management, or related ...
Schnelle Bewerbung
Falk Global Medical (GMED) bridges clinical development and commercial. We translate clinical science and communicate it externally and internally. * Lead the medical TA strategy within the integrated development as well as indication teams * Translate scientific content and clinical data into a logical, scientifically balanced compelling medical story for appropriate audience (presentations, lectures, speaker decks, training courses, publications etc.) * Diverse learning culture and individual development opportunities
Falk Global Medical (GMED) bridges clinical development and commercial. We translate clinical science and communicate it externally and internally. * Lead the medical TA strategy within the integrated development as well as indication teams * Translate scientific content and clinical data into a logical, scientifically balanced compelling medical story for appropriate audience (presentations, lectures, speaker decks, training courses, publications etc.) * Diverse learning culture and individual development opportunities
Global Commercial New Products Manager - 70% part-time (m/f/d)
Global Commercial New Products Manager - 70% part-time (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
Ensure strong cross-functional collaboration with Global Market Access, Medical Affairs, Marketing, Clinical Development, and External Innovation * Develop early go-to-market strategies aligned with stakeholder expectations and commercial goals * Contribute commercial insights into product profiles, lifecycle planning, and early clinical development * Support clinical research, external science, and innovation decision-making through robust commercial assessments * Drive the development of early commercial strategies for selected assets and support global opportunity maximization for Dr. Falk * Support the Business Development and Partnering team in commercial out-licensing activities * 6+ years of experience in Marketing, New Products, Business Development, or related commercial roles in the pharmaceutical/biotech industry
Ensure strong cross-functional collaboration with Global Market Access, Medical Affairs, Marketing, Clinical Development, and External Innovation * Develop early go-to-market strategies aligned with stakeholder expectations and commercial goals * Contribute commercial insights into product profiles, lifecycle planning, and early clinical development * Support clinical research, external science, and innovation decision-making through robust commercial assessments * Drive the development of early commercial strategies for selected assets and support global opportunity maximization for Dr. Falk * Support the Business Development and Partnering team in commercial out-licensing activities * 6+ years of experience in Marketing, New Products, Business Development, or related commercial roles in the pharmaceutical/biotech industry
Projektmanager Klinische Forschung Phase 1 - 3 (m/w/d)
Projektmanager Klinische Forschung Phase 1 - 3 (m/w/d)
Dr. Falk Pharma GmbH
Freiburg im Breisgau
Teilweise Home-Office
Schnelle Bewerbung
Dr. Falk Pharma GmbH * Freiburg im Breisgau * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Als Spezialist in der Verdauungs- und Stoffwechselmedizin und Familienunternehmen mit globaler Vernetzung, setzen wir unseren Fokus auf die Entwicklung und den Vertrieb innovativer Arzneimittel für verschiedene Erkrankungen der Leber, der Gallenwege, des Darms und der Speiseröhre, um das Leben von Menschen zu verbessern. Wir glauben daran, dass wir nur gemeinsam medizinischen Fortschritt erreichen können. Deine Aufgaben - Ihre Aufgaben * Planung, Durchführung und Auswertung internationaler klinischer Zulassungsstudien der Phasen I-III entsprechend den GCP/ICH-Richtlinien sowie EU-Regularien * Erstellung, Durchsicht und Freigabe aller relevanten Studiendokumente in Zusammenarbeit mit externen
Dr. Falk Pharma GmbH * Freiburg im Breisgau * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Als Spezialist in der Verdauungs- und Stoffwechselmedizin und Familienunternehmen mit globaler Vernetzung, setzen wir unseren Fokus auf die Entwicklung und den Vertrieb innovativer Arzneimittel für verschiedene Erkrankungen der Leber, der Gallenwege, des Darms und der Speiseröhre, um das Leben von Menschen zu verbessern. Wir glauben daran, dass wir nur gemeinsam medizinischen Fortschritt erreichen können. Deine Aufgaben - Ihre Aufgaben * Planung, Durchführung und Auswertung internationaler klinischer Zulassungsstudien der Phasen I-III entsprechend den GCP/ICH-Richtlinien sowie EU-Regularien * Erstellung, Durchsicht und Freigabe aller relevanten Studiendokumente in Zusammenarbeit mit externen
){kind=logo}
Schnelle Bewerbung
IGES Institut GmbH * Berlin * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Die IGES GmbH ist auf gesundheitsökonomische und strategische Forschungs- und Beratungsdienstleistungen für internationale Arzneimittel- und Medizinproduktehersteller spezialisiert. Sie bietet Biotech-, Pharma- und Medizinprodukteunternehmen Lösungen für den Market Access, Preisbildung und Erstattung ihrer medizinischen Innovationen. Das Unternehmen ist in Frankreich, Deutschland, Italien, Spanien, Schweden, der Schweiz und Großbritannien vertreten und unterstützt auch bei multinationalen Produkteinführungen. IGES ist Teil der Athagoras Gruppe, die verschiedene Beratungsunternehmen für die Lifescience-Branche vereint. Zur Verstärkung unseres Teams im Bereich Value Strategy & RWE suchen wir zum nächstmöglichen Zeitpunkt an unserem Standort in ...
IGES Institut GmbH * Berlin * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Die IGES GmbH ist auf gesundheitsökonomische und strategische Forschungs- und Beratungsdienstleistungen für internationale Arzneimittel- und Medizinproduktehersteller spezialisiert. Sie bietet Biotech-, Pharma- und Medizinprodukteunternehmen Lösungen für den Market Access, Preisbildung und Erstattung ihrer medizinischen Innovationen. Das Unternehmen ist in Frankreich, Deutschland, Italien, Spanien, Schweden, der Schweiz und Großbritannien vertreten und unterstützt auch bei multinationalen Produkteinführungen. IGES ist Teil der Athagoras Gruppe, die verschiedene Beratungsunternehmen für die Lifescience-Branche vereint. Zur Verstärkung unseres Teams im Bereich Value Strategy & RWE suchen wir zum nächstmöglichen Zeitpunkt an unserem Standort in ...
){kind=logo}
Facharzt Anästhesiologie - südliches Mecklenburg-Vorpommern (m/w/d) - SHC-196-176-MS
Facharzt Anästhesiologie - südliches Mecklenburg-Vorpommern (m/w/d) - SHC-196-176-MS
meinestadt.de
Waren/Müritz
meinestadt.de * Waren/Müritz * Arbeitnehmerüberlassung * Vollzeit - Sei einer der ersten Bewerber - Arbeitgeber: 1a-Ärztevermittlung GmbH - Einsatzort: 17192 Waren/Müritz * Stellenangebot: Facharzt (m/w/d) - Anästhesiologie * Spezialisierung: - keine Angabe - * Arbeitsort: südliches Mecklenburg-Vorpommern - Direkt zum Stellenangebot: Aufgaben - Im Auftrag eines Mandanten suchen wir einen Facharzt (m/w/d) für Anästhesiologie. Bei unserem Auftraggeber handelt es sich um ein Krankenhaus der Grund- und Regelversorgung, mit 12 Hauptabteilungen und einer Größenklasse von 350 - 400 Betten. Die Klinik für Anästhesiologie und Intensivmedizin führt die Vorbereitung, Überwachung und Nachbereitung von Operationen durch. Dabei werden die Patienten anästhesiologisch, wenn nötig intensivmedizinisch und schmerztherapeutisch betreut. Es werden modernste Anästhesieverfahren angewendet.
meinestadt.de * Waren/Müritz * Arbeitnehmerüberlassung * Vollzeit - Sei einer der ersten Bewerber - Arbeitgeber: 1a-Ärztevermittlung GmbH - Einsatzort: 17192 Waren/Müritz * Stellenangebot: Facharzt (m/w/d) - Anästhesiologie * Spezialisierung: - keine Angabe - * Arbeitsort: südliches Mecklenburg-Vorpommern - Direkt zum Stellenangebot: Aufgaben - Im Auftrag eines Mandanten suchen wir einen Facharzt (m/w/d) für Anästhesiologie. Bei unserem Auftraggeber handelt es sich um ein Krankenhaus der Grund- und Regelversorgung, mit 12 Hauptabteilungen und einer Größenklasse von 350 - 400 Betten. Die Klinik für Anästhesiologie und Intensivmedizin führt die Vorbereitung, Überwachung und Nachbereitung von Operationen durch. Dabei werden die Patienten anästhesiologisch, wenn nötig intensivmedizinisch und schmerztherapeutisch betreut. Es werden modernste Anästhesieverfahren angewendet.
){kind=logo}
Schnelle Bewerbung
Kreienbaum Neoscience GmbH * Langenfeld * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Die KREIENBAUM Neoscience GmbH ist ein spezialisiertes medizintechnisches-Vertriebsunternehmen und vertritt exklusiv internationale Hersteller medizinischer Produkte im Krankenhausmarkt. Wir bringen innovative Lösungen in die Klinik und schaffen Mehrwert für Fachpersonal und Patienten. Ein besonderer Schwerpunkt liegt in sensiblen Versorgungsbereichen wie der Neonatologie und Pädiatrie. Dabei verstehen wir uns als verlässliche Schnittstelle zwischen und . Mit Sitz in Langenfeld zwischen Düsseldorf und Köln sind wir bestens angebunden und bundesweit aktiv. Als nach EN ISO 13485:2021 zertifiziertes Unternehmen stehen Qualität, partnerschaftliche Zusammenarbeit und kontinuierliche Weiterentwicklung im Mittelpunkt unseres Handelns.
Kreienbaum Neoscience GmbH * Langenfeld * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Die KREIENBAUM Neoscience GmbH ist ein spezialisiertes medizintechnisches-Vertriebsunternehmen und vertritt exklusiv internationale Hersteller medizinischer Produkte im Krankenhausmarkt. Wir bringen innovative Lösungen in die Klinik und schaffen Mehrwert für Fachpersonal und Patienten. Ein besonderer Schwerpunkt liegt in sensiblen Versorgungsbereichen wie der Neonatologie und Pädiatrie. Dabei verstehen wir uns als verlässliche Schnittstelle zwischen und . Mit Sitz in Langenfeld zwischen Düsseldorf und Köln sind wir bestens angebunden und bundesweit aktiv. Als nach EN ISO 13485:2021 zertifiziertes Unternehmen stehen Qualität, partnerschaftliche Zusammenarbeit und kontinuierliche Weiterentwicklung im Mittelpunkt unseres Handelns.
){kind=logo}
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 ...
){kind=logo}
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
Schnelle Bewerbung
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
){kind=logo}
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental ...
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental ...
){kind=logo}
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.
){kind=logo}
ZEISS * Oberkochen - Sei einer der ersten Bewerber - Seeing beyond - future of medical technology - Seit mehr als 100 Jahren treibt die Medizintechnik von ZEISS den Fortschritt in der Augenheilkunde und Mikrochirurgie voran. In der Augenheilkunde unterstützen unsere Lösungen dabei, die Sehkraft von Menschen zu jedem Zeitpunkt des Lebens zu erhalten und zu verbessern. In der Mikrochirurgie ermöglichen unsere Lösungen gezielte Eingriffe am erkrankten Gewebe, sodass kleine und empfindliche Organe weiterhin optimal funktionieren. Die Medizintechnik von ZEISS unterstützt medizinische Fachkräfte dabei, das Leben von Patientinnen und Patienten weltweit zu verbessern. Dass wir mit unserem Tun einen direkten Einfluss auf das Wohl der Menschen haben, ist unser täglicher Antrieb. Wir suchen eine engagierte Person, die in Ostdeutschland (neue Bundesländer) ansässig ist. Ihre Rolle
ZEISS * Oberkochen - Sei einer der ersten Bewerber - Seeing beyond - future of medical technology - Seit mehr als 100 Jahren treibt die Medizintechnik von ZEISS den Fortschritt in der Augenheilkunde und Mikrochirurgie voran. In der Augenheilkunde unterstützen unsere Lösungen dabei, die Sehkraft von Menschen zu jedem Zeitpunkt des Lebens zu erhalten und zu verbessern. In der Mikrochirurgie ermöglichen unsere Lösungen gezielte Eingriffe am erkrankten Gewebe, sodass kleine und empfindliche Organe weiterhin optimal funktionieren. Die Medizintechnik von ZEISS unterstützt medizinische Fachkräfte dabei, das Leben von Patientinnen und Patienten weltweit zu verbessern. Dass wir mit unserem Tun einen direkten Einfluss auf das Wohl der Menschen haben, ist unser täglicher Antrieb. Wir suchen eine engagierte Person, die in Ostdeutschland (neue Bundesländer) ansässig ist. Ihre Rolle
){kind=logo}
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 4271 weitere Jobs, die zu deiner Suche passen könnten
){kind=logo}
Field Clinical Specialist - Imaging
Field Clinical Specialist - Imaging
Edwards Lifesciences GmbH
Nordrhein-Westfalen, Rheinland-Pfalz
Teilweise Home-Office
Schnelle Bewerbung
Analyze, summarize, and present clinical baseline, procedural, and follow-up imaging (e.g., CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations - Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. The Field Clinical Specialist - Imaging is responsible for educating physicians on EVOQUE technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals / in assigned territories / regions. * Provide on-site cardiac imaging support and guidance during clinical procedures to ensure optimal imaging during the implantation of transcatheter devices (if certified). * Bachelor's Degree in in technical field (e.g., clinical physiology, ...
Analyze, summarize, and present clinical baseline, procedural, and follow-up imaging (e.g., CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations - Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. The Field Clinical Specialist - Imaging is responsible for educating physicians on EVOQUE technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals / in assigned territories / regions. * Provide on-site cardiac imaging support and guidance during clinical procedures to ensure optimal imaging during the implantation of transcatheter devices (if certified). * Bachelor's Degree in in technical field (e.g., clinical physiology, ...
Field Clinical Specialist TMTT, Bonn/Siegen
Field Clinical Specialist TMTT, Bonn/Siegen
Edwards Lifesciences GmbH
Bonn, Siegen
Teilweise Home-Office
Schnelle Bewerbung
Your insight and dedication will help deepen and broaden clinical knowledge of our company's innovative technologies, while creating connections between and teams across our businesses to ensure patients receive the highest quality of care. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. * Regularly reviews clinical support activities and changes in the market & assigned accounts * Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. * Bachelor's Degree in related field (Biomedical Engineering or Nursing) and training experience in clinical / technical environment is required. * Clinical experience is beneficial
Your insight and dedication will help deepen and broaden clinical knowledge of our company's innovative technologies, while creating connections between and teams across our businesses to ensure patients receive the highest quality of care. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. * Regularly reviews clinical support activities and changes in the market & assigned accounts * Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. * Bachelor's Degree in related field (Biomedical Engineering or Nursing) and training experience in clinical / technical environment is required. * Clinical experience is beneficial
Field Clinical Specialist Münster - Hannover
Field Clinical Specialist Münster - Hannover
Edwards Lifesciences GmbH
Bielefeld, Münster, Hannover
Teilweise Home-Office
Schnelle Bewerbung
Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Field Clinical Specialists will provide guidance on the use of the device, thereby enabling physicians and staff to reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. * Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical education programs
Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Field Clinical Specialists will provide guidance on the use of the device, thereby enabling physicians and staff to reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. * Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical education programs
Project Manager Pre-Clinical Research / Toxicology (m/f/d)
Project Manager Pre-Clinical Research / Toxicology (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
You will contribute to the translational development of drug candidates and ensure the scientific and regulatory integrity of all preclinical data packages. * Comprehensive data interpretation, including assessment of pharmacological and toxicological endpoints, integration of findings across studies, and development of scientifically substantiated conclusions * Systematic literature research and integration of external evidence into internal development strategies * Several years of industry experience in pharmacological or toxicological research (ideally in drug development) * Diverse learning culture and individual development opportunities
You will contribute to the translational development of drug candidates and ensure the scientific and regulatory integrity of all preclinical data packages. * Comprehensive data interpretation, including assessment of pharmacological and toxicological endpoints, integration of findings across studies, and development of scientifically substantiated conclusions * Systematic literature research and integration of external evidence into internal development strategies * Several years of industry experience in pharmacological or toxicological research (ideally in drug development) * Diverse learning culture and individual development opportunities
){kind=logo}
Schnelle Bewerbung
ORGENTEC Diagnostika GmbH is the global market leader in the development and production of test systems for the diagnosis of infectious and autoimmune diseases. * Support the creation of templates for Clinical Evidence requirements * Individualised employee development and training
ORGENTEC Diagnostika GmbH is the global market leader in the development and production of test systems for the diagnosis of infectious and autoimmune diseases. * Support the creation of templates for Clinical Evidence requirements * Individualised employee development and training
){kind=logo}
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
){kind=logo}
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
){kind=logo}
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
Beliebte Jobs
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Stuttgart
- Düsseldorf
- Hannover
- Leipzig
- Dresden
- Nürnberg
- Essen
- Karlsruhe
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Ulm
- Heidelberg
- Walldorf, Baden-Württemberg
- Gilching
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Niederrhein
- Taunus
- Oberbayern