Schnelle Bewerbung
162
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
- Dresden
- Nürnberg
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Augsburg
- Freiburg im Breisgau
- Duisburg
- Kassel
- Heidelberg
- Trier
- Calw
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Schwarzwald
- Taunus
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
- Dresden
- Nürnberg
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Augsburg
- Freiburg im Breisgau
- Duisburg
- Kassel
- Heidelberg
- Trier
- Calw
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Schwarzwald
- Taunus
379 Treffer für Clinical Affairs Jobs
){kind=logo}
Associate Director Regulatory Affairs – Clinical Lead*
Associate Director Regulatory Affairs – Clinical Lead*
Immatics Biotechnologies GmbH
Tübingen, München, Home-Office
Teilweise Home-Office
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications. * Master's degree in natural sciences (e.g. Biology, Chemistry or Pharmacy) or Regulatory Affairs * 8+ years of Regulatory Affairs experience in biopharmaceuticals and/or ATMPs. * Demonstrated experience leading EU regulatory strategy for clinical-stage programs.
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications. * Master's degree in natural sciences (e.g. Biology, Chemistry or Pharmacy) or Regulatory Affairs * 8+ years of Regulatory Affairs experience in biopharmaceuticals and/or ATMPs. * Demonstrated experience leading EU regulatory strategy for clinical-stage programs.
){kind=logo}
Schnelle Bewerbung
Für unseren Firmenstandort Leipzig suchen wir ein Senior Clinical Affairs Manager (m/w/d)en * Erfahrungen in der Planung und Durchführung nationaler und internationaler klinischer Studien als CRA, Clinical Trialoder Projektmanager in der Medizintechnik oder ähnlichen Branchen
Für unseren Firmenstandort Leipzig suchen wir ein Senior Clinical Affairs Manager (m/w/d)en * Erfahrungen in der Planung und Durchführung nationaler und internationaler klinischer Studien als CRA, Clinical Trialoder Projektmanager in der Medizintechnik oder ähnlichen Branchen
){kind=logo}
In unserem Clinical Affairs Team unterstützen Sie Rund um den Einsatz von lebensrettenden Herzunterstützungssystemen für Kinder. Für unser international agierendes Supportteam suchen wir einen Clinical Specialist m/w/d * Clinical Support im Rahmen von Implantationen unserer Unterstützungssysteme
In unserem Clinical Affairs Team unterstützen Sie Rund um den Einsatz von lebensrettenden Herzunterstützungssystemen für Kinder. Für unser international agierendes Supportteam suchen wir einen Clinical Specialist m/w/d * Clinical Support im Rahmen von Implantationen unserer Unterstützungssysteme
Enge Zusammenarbeit mit dem Clinical Team, Medical Affairs und unserem Innendienst - Stellenausschreibung – Clinical Diabetes Sales Specialist (m/w/d) Wir suchen: Clinical Diabetes Sales Specialist (m/w/d) – Region Bayern
Enge Zusammenarbeit mit dem Clinical Team, Medical Affairs und unserem Innendienst - Stellenausschreibung – Clinical Diabetes Sales Specialist (m/w/d) Wir suchen: Clinical Diabetes Sales Specialist (m/w/d) – Region Bayern
){kind=logo}
Country Marketing Manager, TMTT Germany
Country Marketing Manager, TMTT Germany
Edwards Lifesciences GmbH
Bayern, europaweit
Teilweise Home-Office
Schnelle Bewerbung
Partner closely with Medical Affairs, Clinical, and Commercial on segmentation, KOL engagement pathways, and strategic partnerships within the German cardiology community. * 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. * Understand customer and commercial teams' needs through regular field presence, localize marketing assets, and develop thorough knowledge of therapy, clinical data and competitive landscape * Possess strong clinical knowledge, experience and knowledge of the clinical areas where Edwards' products are used or intended to be used, understand the purchasing process and challenges for product adoption in complex healthcare networks
Partner closely with Medical Affairs, Clinical, and Commercial on segmentation, KOL engagement pathways, and strategic partnerships within the German cardiology community. * 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. * Understand customer and commercial teams' needs through regular field presence, localize marketing assets, and develop thorough knowledge of therapy, clinical data and competitive landscape * Possess strong clinical knowledge, experience and knowledge of the clinical areas where Edwards' products are used or intended to be used, understand the purchasing process and challenges for product adoption in complex healthcare networks
){kind=logo}
Schnelle Bewerbung
• Collaborate closely with clinical development, regulatory affairs, CMC, nonclinical, safety, biomarker, and business development colleagues. HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. 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. The role requires someone who has worked in or closely with the pharmaceutical industry and understands how development decisions are made under real-world constraints of time, budget, regulatory risk, and clinical feasibility.
• Collaborate closely with clinical development, regulatory affairs, CMC, nonclinical, safety, biomarker, and business development colleagues. HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. 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. The role requires someone who has worked in or closely with the pharmaceutical industry and understands how development decisions are made under real-world constraints of time, budget, regulatory risk, and clinical feasibility.
Field Clinical Specialist Münster - Hannover
Field Clinical Specialist Münster - Hannover
Edwards Lifesciences GmbH
Bielefeld, Münster, Hannover
Teilweise Home-Office
Schnelle Bewerbung
This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. 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. 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
This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. 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. 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
){kind=logo}
Senior Consultant Arzneimittel - Pharmacovigilance (m/w/d)
Senior Consultant Arzneimittel - Pharmacovigilance (m/w/d)
TentaConsult Pharma & Med GmbH
Münster, Martinsried
Teilweise Home-Office
Schnelle Bewerbung
Unser Tätigkeitsfeld umfasst Leistungen in den Bereichen Regulatory & Clinical, Biological Affairs und Qualitätsmanagement.
Unser Tätigkeitsfeld umfasst Leistungen in den Bereichen Regulatory & Clinical, Biological Affairs und Qualitätsmanagement.
Schnelle Bewerbung
Erste Erfahrung im Marketing, Produktmanagement oder Clinical Affairs innerhalb der Medizintechnik/ Pharmaindustrie von Vorteil
Erste Erfahrung im Marketing, Produktmanagement oder Clinical Affairs innerhalb der Medizintechnik/ Pharmaindustrie von Vorteil
NEU
){kind=logo}
Domain-naher QA-Experte - Life Sciences (m/w/d)
Domain-naher QA-Experte - Life Sciences (m/w/d)
SPIRIT-TESTING Software & Services GmbH
München
Teilweise Home-Office
In dieser Rolle bringen Sie tiefes Domänenwissen aus den Life Sciences (z. B. klinische Studien, Regulatory Affairs, MedTech-Produktentwicklung oder Laborprozesse) mit einem klaren Fokus auf Software- und Systemqualität zusammen. * Clinical Operations * Regulatory Affairs
In dieser Rolle bringen Sie tiefes Domänenwissen aus den Life Sciences (z. B. klinische Studien, Regulatory Affairs, MedTech-Produktentwicklung oder Laborprozesse) mit einem klaren Fokus auf Software- und Systemqualität zusammen. * Clinical Operations * Regulatory Affairs
Noch nichts dabei? Es gibt 369 weitere Jobs, die zu deiner Suche passen könnten
){kind=logo}
Oversee the planning, execution, and maintenance of clinical evaluation activities to ensure compliance with regulatory requirements and company standards * Collate and analyze clinical data from clinical trials and testing, scientific literature, and post-market experience * Create, edit, and proofread Clinical Evaluation Reports and associated documents to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations * Experience in regulatory affairs is beneficial * Understanding of, and enthusiasm for scientific working, medical technology, and clinical research
Oversee the planning, execution, and maintenance of clinical evaluation activities to ensure compliance with regulatory requirements and company standards * Collate and analyze clinical data from clinical trials and testing, scientific literature, and post-market experience * Create, edit, and proofread Clinical Evaluation Reports and associated documents to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations * Experience in regulatory affairs is beneficial * Understanding of, and enthusiasm for scientific working, medical technology, and clinical research
NEU
){kind=logo}
Schnelle Bewerbung
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.). Senior Scientific Affairs Manager (m/f/d) The role acts as a central interface between scientific/clinical, QARA, Sales, Marketing and Strategy. * Statistical analysis and evaluation of clinical data (hands-on) * Management, support and coordination of in the preparation and maintenance of clinical evaluations * Support scientific/ regulatory affairs teams worldwide with product registration * Review, adapt/ improve scientific affairs processes regularly
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.). Senior Scientific Affairs Manager (m/f/d) The role acts as a central interface between scientific/clinical, QARA, Sales, Marketing and Strategy. * Statistical analysis and evaluation of clinical data (hands-on) * Management, support and coordination of in the preparation and maintenance of clinical evaluations * Support scientific/ regulatory affairs teams worldwide with product registration * Review, adapt/ improve scientific affairs processes regularly
){kind=logo}
Wenn Sie jetzt denken „Hier ist meine Zukunft!", dann freuen wir uns auf Ihre Bewerbung als Medical Affairs Lead (m/w/d) Amyloidosis. * Sicherstellung von Synergien innerhalb von Medical Affairs CVRM und Amyloidose (national und international) und crossfunktional * Unterstützung der Implementierung und Durchführung von AZ-gesponsorten Studien in Zusammenarbeit mit Clinical Operations * Erfahrung in der klinischen Forschung und/oder Medical Affairs & Education, bevorzugt mit Fokus Neurologie, Kardiologie oder Herzinsuffizienz.
Wenn Sie jetzt denken „Hier ist meine Zukunft!", dann freuen wir uns auf Ihre Bewerbung als Medical Affairs Lead (m/w/d) Amyloidosis. * Sicherstellung von Synergien innerhalb von Medical Affairs CVRM und Amyloidose (national und international) und crossfunktional * Unterstützung der Implementierung und Durchführung von AZ-gesponsorten Studien in Zusammenarbeit mit Clinical Operations * Erfahrung in der klinischen Forschung und/oder Medical Affairs & Education, bevorzugt mit Fokus Neurologie, Kardiologie oder Herzinsuffizienz.
){kind=logo}
Packaging & Labeling Specialist (m/w/d) Pharma, Clinical Trials & Verpackungsmanagement
Packaging & Labeling Specialist (m/w/d) Pharma, Clinical Trials & Verpackungsmanagement
expertum GmbH
Biberach an der Riß
Anschreiben nicht erforderlich
Schnelle Bewerbung
Clinical Trials, Clinical Supply, Packaging, Labeling, Regulatory Affairs, Qualitätsmanagement, Projektmanagement oder Supply Chain Management - Packaging & Labeling Specialist / Clinical Supply Specialist (m/w/d) - Pharma, Clinical Trials & Verpackungsmanagement - Mitwirkung bei der Weiterentwicklung und Optimierung von Prozessen, Technologien und Arbeitsabläufen im Clinical Development Umfeld
Clinical Trials, Clinical Supply, Packaging, Labeling, Regulatory Affairs, Qualitätsmanagement, Projektmanagement oder Supply Chain Management - Packaging & Labeling Specialist / Clinical Supply Specialist (m/w/d) - Pharma, Clinical Trials & Verpackungsmanagement - Mitwirkung bei der Weiterentwicklung und Optimierung von Prozessen, Technologien und Arbeitsabläufen im Clinical Development Umfeld
NEU
Sicherstellung von Synergien innerhalb von Medical Affairs Oncology (national und international) und x-funktional * Medizinisch-wissenschaftliche Verantwortung für die strategische Entwicklung und Durchführung von LCM-Projekten und lokalen und globalen (Medical Affairs) medizinischen Projekten (z.B. lokale klinische Studien, NIS) * Unterstützung der Implementierung und Durchführung von AZ-gesponsorten Studien in Zusammenarbeit mit Clinical Operations * Erfahrung in der Zusammenarbeit mit Clinical Operations und Zulassung sowie mit Studiengruppen und extern gesponsorten Studien
Sicherstellung von Synergien innerhalb von Medical Affairs Oncology (national und international) und x-funktional * Medizinisch-wissenschaftliche Verantwortung für die strategische Entwicklung und Durchführung von LCM-Projekten und lokalen und globalen (Medical Affairs) medizinischen Projekten (z.B. lokale klinische Studien, NIS) * Unterstützung der Implementierung und Durchführung von AZ-gesponsorten Studien in Zusammenarbeit mit Clinical Operations * Erfahrung in der Zusammenarbeit mit Clinical Operations und Zulassung sowie mit Studiengruppen und extern gesponsorten Studien
Schnelle Bewerbung
Engage and coordinate with cross-functional teams (Marketing, Medical Affairs, Customer Service, Bids & Tenders, Finance, HR, Legal, etc.) demonstrating a mature understanding of their potential role in contributing to the customer experience and where needed takes the lead in enrolling these functions in deploying tailored customer-centric solutions. * 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 .
Engage and coordinate with cross-functional teams (Marketing, Medical Affairs, Customer Service, Bids & Tenders, Finance, HR, Legal, etc.) demonstrating a mature understanding of their potential role in contributing to the customer experience and where needed takes the lead in enrolling these functions in deploying tailored customer-centric solutions. * 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 .
){kind=logo}
We are looking for a Payer Value Demonstration Specialist to join the Global Market Access team, which consists of nine members and operates within the Clinical Operations division. * Engage with global market access and Medical Affairs team
We are looking for a Payer Value Demonstration Specialist to join the Global Market Access team, which consists of nine members and operates within the Clinical Operations division. * Engage with global market access and Medical Affairs team
){kind=logo}
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. 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.
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. 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.
){kind=logo}
Schnelle Bewerbung
Director of Medical Affairs provides scientific and medical leadership to establish a deep understanding of the medical landscape regarding relevant, rare amyloidoses, such as AL-A, and Alexion products. Director of Medical Affairs Amyloidosis makes strategic contributions to Alexion's activities in the field of rare amyloidoses. They support all functions of the German subsidiary working in this field in achieving local targets and Alexion Global Medical Affairs in its mission to achieve treatment outcomes by establishing and continuously improving an evidence-based standard of medical care. * Disciplinary leadership of the Amyloidosis Medical Affairs team and ensuring the team's objectives are achieved through the efficient management of all directly reporting to the position and the retention of talented employees through personal development support.
Director of Medical Affairs provides scientific and medical leadership to establish a deep understanding of the medical landscape regarding relevant, rare amyloidoses, such as AL-A, and Alexion products. Director of Medical Affairs Amyloidosis makes strategic contributions to Alexion's activities in the field of rare amyloidoses. They support all functions of the German subsidiary working in this field in achieving local targets and Alexion Global Medical Affairs in its mission to achieve treatment outcomes by establishing and continuously improving an evidence-based standard of medical care. * Disciplinary leadership of the Amyloidosis Medical Affairs team and ensuring the team's objectives are achieved through the efficient management of all directly reporting to the position and the retention of talented employees through personal development support.
){kind=logo}
Special Operations Licensed Clinical Social Worker (Stuttgart, Germany)
Special Operations Licensed Clinical Social Worker (Stuttgart, Germany)
Kellogg Brown & Root GmbH
Stuttgart, Baden-Wurttemberg, Germany
We are looking for a Special OperationsLicensed Clinical Social Worker to join the team who is responsible for integrating the physical, mental and psychological wellness of our service members and their families. This Special Operations Licensed Clinical Social Worker will function within an operational unit, as a Behavioral Health Care Provider and is responsible for the application of social work procedures and techniques, including interviewing, behavioral assessment, and evidenced-based therapies, in the evaluation, diagnosis, and treatment of psychological and neuropsychological disorders using the following skills: individual, family and group psychotherapy, couple's therapy, alcohol and drug treatment evaluations. * Conduct applied research and clinical investigations in clinical/behavioral health/organizational social work.
We are looking for a Special OperationsLicensed Clinical Social Worker to join the team who is responsible for integrating the physical, mental and psychological wellness of our service members and their families. This Special Operations Licensed Clinical Social Worker will function within an operational unit, as a Behavioral Health Care Provider and is responsible for the application of social work procedures and techniques, including interviewing, behavioral assessment, and evidenced-based therapies, in the evaluation, diagnosis, and treatment of psychological and neuropsychological disorders using the following skills: individual, family and group psychotherapy, couple's therapy, alcohol and drug treatment evaluations. * Conduct applied research and clinical investigations in clinical/behavioral health/organizational social work.
){kind=logo}
Schnelle Bewerbung
• Clinical Evaluation Reports (CER) * Erste bis mehrjährige Erfahrung im Bereich Regulatory Affairs für Medizinprodukte (idealerweise Klasse IIa oder höher)
• Clinical Evaluation Reports (CER) * Erste bis mehrjährige Erfahrung im Bereich Regulatory Affairs für Medizinprodukte (idealerweise Klasse IIa oder höher)
){kind=logo}
Release Engineer / Technical Lead, Software & Electronics (m/w/d)
Release Engineer / Technical Lead, Software & Electronics (m/w/d)
Ambu Innovation
Augsburg
Teilweise Home-Office
Would you like to take a leading role in bringing regulated AI solutions safely and efficiently into clinical use? You will combine deep technical understanding with a strong design control discipline, acting as the technical anchor between AI/ML developers, system engineers, quality, regulatory affairs, and project management. * Translating clinical, business, and regulatory needs into robust technical requirements.
Would you like to take a leading role in bringing regulated AI solutions safely and efficiently into clinical use? You will combine deep technical understanding with a strong design control discipline, acting as the technical anchor between AI/ML developers, system engineers, quality, regulatory affairs, and project management. * Translating clinical, business, and regulatory needs into robust technical requirements.
){kind=logo}
Schnelle Bewerbung
die Enge Zusammenarbeit mit Clinical Research zur Ableitung relevanter Studienansätze und zur Nutzung klinischer Daten für Produktstrategie und Zulassungen * die Steuerung von Produktentwicklungs- und Optimierungsprojekten in enger Abstimmung mit F&E, QM und Regulatory Affairs
die Enge Zusammenarbeit mit Clinical Research zur Ableitung relevanter Studienansätze und zur Nutzung klinischer Daten für Produktstrategie und Zulassungen * die Steuerung von Produktentwicklungs- und Optimierungsprojekten in enger Abstimmung mit F&E, QM und Regulatory Affairs
Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. Für den weiteren Ausbau der Prozessdomäne Regulatory Affairs suchen wir zum nächstmöglichen Zeitpunkt eine erfahrene Persönlichkeit als Head of Regulatory Consulting. * Aufbau, Weiterentwicklung und Positionierung unserer Beratungsansätze im Bereich Regulatory Affairs * Enge Zusammenarbeit mit angrenzenden Disziplinen (z.B. Clinical) * Fundierte Branchenkenntnisse in der Life-Science-Industrie, insbesondere im Umfeld Regulatory Affairs und relevanter IT-Systemlandschaften * Mindestens 10 Jahre Berufserfahrung in Regulatory Affairs, Beratung oder angrenzenden Bereichen, davon mindestens 3 Jahre in leitender Funktion
Unsere Kunden begleiten wir von der Strategie bis zur erfolgreichen Umsetzung entlang der Prozessdomänen Clinical Operations & Data Management, Regulatory Affairs, Quality und Manufacturing. Für den weiteren Ausbau der Prozessdomäne Regulatory Affairs suchen wir zum nächstmöglichen Zeitpunkt eine erfahrene Persönlichkeit als Head of Regulatory Consulting. * Aufbau, Weiterentwicklung und Positionierung unserer Beratungsansätze im Bereich Regulatory Affairs * Enge Zusammenarbeit mit angrenzenden Disziplinen (z.B. Clinical) * Fundierte Branchenkenntnisse in der Life-Science-Industrie, insbesondere im Umfeld Regulatory Affairs und relevanter IT-Systemlandschaften * Mindestens 10 Jahre Berufserfahrung in Regulatory Affairs, Beratung oder angrenzenden Bereichen, davon mindestens 3 Jahre in leitender Funktion
){kind=logo}
Applikation Spezialist für Photon-Counting CT (m/w/d)
Applikation Spezialist für Photon-Counting CT (m/w/d)
AB-CT - Advanced Breast-CT GmbH
Erlangen
Teilweise Home-Office
Schnelle Bewerbung
Mitwirkung bei der klinischen Bewertung sowie Unterstützung von Post-Market Surveillance (PMS) und Post-Market Clinical Follow-up (PMCF) - Enge Zusammenarbeit mit Produktmanagement, Service, Entwicklung sowie Regulatory Affairs
Mitwirkung bei der klinischen Bewertung sowie Unterstützung von Post-Market Surveillance (PMS) und Post-Market Clinical Follow-up (PMCF) - Enge Zusammenarbeit mit Produktmanagement, Service, Entwicklung sowie Regulatory Affairs
NEU
Beliebte Jobs
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Stuttgart
- Düsseldorf
- Hannover
- Dresden
- Nürnberg
- Dortmund
- Münster, Nordrhein-Westfalen
- Bonn
- Augsburg
- Freiburg im Breisgau
- Duisburg
- Kassel
- Heidelberg
- Trier
- Calw
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Südbayern
- Schwarzwald
- Taunus