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Neu Job vor 7 Std. gefunden Aesculap AG part of the B. Braun Group

Internship (w/m/d) Usability/ Human Factors Engineer

• Tuttlingen
MEHR[...] and summative usability evaluations and recommend optimizations. You support the development of all necessary usability- related documents according to IEC 62366- 1 and FDA Guidance Documents You support the usability- related risk analysis according to ISO 14971. You collaborate with clinical advisors, healthcare professionals, risk managers, quality managers, UX UI designers, UX researchers, and developers Professional competencies Currently enrolled and successfully completed at least 2 years of study, preferably in Human Factors Engineering, Psychology Engineering, Product Design, UX UI Design, or Medical Engineering Initial experience (e. g. , [...]
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Job gestern gefunden Exact Sciences Research Scientist I, Germany • Munich
MEHR[...] a project. Participate in the development of research plans and experimental outlines, write experimental protocols, and perform laboratory experiments. Prepare detailed technical procedures, protocols, and reports. Evaluate impact of nonconforming data to product or process. Identify and address trends in study data. Prepare and approve written reports. Lead identification of areas for process improvements. Maintain lab notebook in a complete and [...] freezing elements, and high- speed centrifugation. Ability and means to travel between local Exact Sciences locations. Ability to travel 5 of working time away from work location, may include overnight/ weekend travel. Minimum Qualifications PhD in life sciences, medical technology, clinical laboratory science, chemical/ physical/ biological science, or related field; or Master s degree in life sciences, medical technology, clinical laboratory [...]
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Job gestern gefunden Exact Sciences

Research Scientist I, Germany

• Planegg
MEHR[...] a project. Participate in the development of research plans and experimental outlines, write experimental protocols, and perform laboratory experiments. Prepare detailed technical procedures, protocols, and reports. Evaluate impact of nonconforming data to product or process. Identify and address trends in study data. Prepare and approve written reports. Lead identification of areas for process improvements. Maintain lab notebook in a complete and [...] freezing elements, and high- speed centrifugation. Ability and means to travel between local Exact Sciences locations. Ability to travel 5 of working time away from work location, may include overnight/ weekend travel. Minimum Qualifications PhD in life sciences, medical technology, clinical laboratory science, chemical/ physical/ biological science, or related field; or Master s degree in life sciences, medical technology, clinical laboratory [...]
Stellenangebot Clinical Study Job bei Oxford Global Resources Job vor 3 Tagen gefunden Oxford Global Resources Freelance CRA- Medical Devices (German/ English) • Frankfurt Freiberuflich
MEHR[...] would have 0. 7 to 1 FTE availability to give them support in managing sites in Germany, Switzerland and Austria. Remote opportunity + Up to 80 travel is possible. Job Description As a CRA you will be responsible for managing clinical activities at study sites conducting studies for Medical Devices. You will perform site management and monitoring activities and act as the main line [...]
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Job vor 8 Tagen gefunden Universitätsklinikum Bonn

CRA (Clinical Research Associate) - Klinischer Monitor/ Projektkoordinator (m/w/d)

• 53127, Bonn, Deutschland Abgeschlossenes Studium Abgeschlossene Ausbildung Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket
MEHR[...] und weist den dritthöchsten Case Mix Index (Fallschweregrad) in Deutschland auf. In der Studienzentrale SZB des Instituts für Klinische Chemie und Klinische Pharmakologie des Universitätsklinikums Bonn ist ab sofort folgende Stelle in Vollzeit (38, 5 Std./ Woche) zu besetzen: CRA (Clinical Research Associate) Klinischer Monitor/ Projektkoordinator (m/w/d) Die Stelle ist zunächst bis 30. 06. 2026 befristet aufgrund von projektbezogenen Tätigkeiten, eine [...] Parteien (Kontakt zu den Prüfzentren) , Dokumentenerstellung im Rahmen der Vorbereitung und Durchführung klinischer Studien Erstellung von Manualen, Einwilligungserklärungen, Risikoanalysen und Logs Ihr Profil: Abgeschlossene Ausbildung im Gesundheitswesen (Krankenschwester o. ä. ) oder vergleichbare Ausbildung bzw. Studium Abgeschlossene Weiterbildung zur Study Nurse von Vorteil Weiterbildung zum Klinischen Monitor von Vorteil Berufliche Vorerfahrung in der Betreuung und im Monitoring von klinischen Studien [...]
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Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG Regulatory Affairs Manager for Clinical Evaluation (f/m/d) • Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
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Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG

Natural Scientist as Clinical Evaluation Manager (f/m/d)

• Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG Clinical Research Manager for Regulatory Affairs (f/m/d) • Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
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Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG

Regulatory Affairs Manager for Post- Market Surveillance (f/m/d)

• Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG Clinical Evaluation Manager (f/m/d) • Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG

Life Scientist as Clinical Evaluation Manager (f/m/d)

• Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
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Stellenangebot Clinical Study Job bei PAUL HARTMANN AG Neu Job vor 7 Std. gefunden PAUL HARTMANN AG Regulatory Affairs Manager (f/m/d) • Heidenheim
MEHR[...] grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills [...] Identify equivalence to existing devices, if required, in accordance with MDRs and relevant MDCGs. Conduct literature searches and reviews in according to MDR/ MEDDEV 2. 7. 1 rev. 4 Provide searches in relevant vigilance databases Support for risk analysis and study planning for CE and PMCF studies Qualification: University degree in life science/ natural science or an equivalent qualification Professional experience [...]
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Stellenangebot Clinical Study Job bei Immundiagnostik AG Job vom 25.10.2024 Immundiagnostik AG

Clinical Affairs Manager (m/w/d)

Abgeschlossenes Studium
MEHR[...] zur Differenzialdiagnostik sowie zur Therapiekontrolle. Unsere Produkte umfassen Immunoassays (z. B. ELISA, LFA, PETIA) , LC- MS/ MS- und HPLC- Applikationen, molekularbiologische Tests (PCR) sowie photometrische Verfahren. Weitere Informationen über uns finden Sie unter www. immundiagnostik. com. Ab sofort gesucht: Clinical Affairs Manager (m/w/d) in Vollzeit Ref. : 2024- 10- QM- 02 Ihre Aufgaben: Entwicklung und Verwaltung von Protokollen für klinische [...] Sie Eigeninitiative, Kommunikationsstärke, Zuverlässigkeit und Belastbarkeit sowie eine strukturierte und lösungsorientierte Arbeitsweise ( Out of the box thinking ) mitbringen, freuen wir uns auf Ihre Bewerbung. . Mediziner Arzt Dr. med. Medizintechnik Planung Regulatory Affairs klinischen Studien Clinical Affairs Manager Study Nurse Medizinprodukte klinische Daten Studiendurchführung Biologe Naturwissenschaftler 16314334 [...]
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