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Drug Regulatory Affairs Jobs

1 - 12 von 12
1 - 12 von 12
Suchergebnisse - Drug Regulatory Affairs Jobs
apartmentBroeder Ruckh Consulting GmbHplaceAachenlanguagemindmatch.aievent_available
/// Ihr Profil  •  Mindestens 5 Jahre Erfahrung im Bereich (Drug) Regulatory Affairs  •  Kenntnisse des EU-Regulierungsrahmens  •  Regulatorisches Lebenszyklusmanagement im Hinblick auf geschäftliche Anforderungen (CP, DCP, MRP, NP)  •  Idealerweise Kenntnisse der EU...
apartmentRocheplaceStuttgartlanguageroche.comevent_available
trägst Du so direkt dazu bei, die Zukunft des Gesundheitswesens verantwortungsvoll und nachhaltig zu gestalten. Dein neues Team: Du leitest ein engagiertes Team von Expert:innen in der Abteilung Drug Regulatory Affairs (DRA), das durch Kooperation...
6 ähnliche Jobs: Ulm, Freiburg, Mannheim, Heidelberg, Karlsruhe...
apartmentBionorica AGplaceNeumarkt in der Oberpfalzlanguagefinest-jobs.comevent_available
Branche im Bereich International Regulatory Affairs  •  Sehr gute Englisch- und Deutschkenntnisse in Wort und Schrift, weitere Sprachen wie z.B.  •  Chinesisch, Portugiesisch, Spanisch, Arabisch wären wünschenswert  •  Hervorragende Kommunikationsstärke...
apartmentOtsuka Pharma GmbHplaceFrankfurt am Mainlanguagestepstone.deevent_available
that combines Japanese and Western values. An inspiring environment for people who are open to innovation and creativity and want to make a difference together For Otsuka Pharma GmbH in the department Global Regulatory Affairs we are looking for a...
apartmentImmunic AGplaceGräfelfinglanguageappcast.ioevent_available
board and investigators, and representing the study at scientific meetings.  •  Cross-Functional Collaboration: Work closely with Clinical Operations, Regulatory Affairs, Medical Affairs, and Commercial teams to align on study milestones, data readouts...
apartmentBroeder Ruckh Consulting GmbHplaceAachenlanguagejoin.comevent_available
Qualifikation  •  Mindestens 5 Jahre Erfahrung im Bereich (Drug) Regulatory Affairs  •  Kenntnisse des EU-Regulierungsrahmens  •  Regulatorisches Lebenszyklusmanagement im Hinblick auf geschäftliche Anforderungen (CP, DCP, MRP, NP)  •  Idealerweise Kenntnisse der EU...
apartmentJazz PharmaceuticalsplaceMünchenlanguageappcast.ioevent_available
and external stakeholder in various forums and conferences and may interact with regulatory agencies on matters related to Jazz’s products. The Senior Director will be asked to think outside the box to innovate, collaborate, and enhance the medical affairs...
apartmentageneo Life Science Experts (Interim Solutions) GmbHplaceDeutschlandlanguagemindmatch.aievent_available
developmental compounds.  •  Collaborating with Global Epidemiology and Medical Affairs to design safety-oriented post-authorization studies.  •  Analyzing clinical trial safety data for incorporation into clinical trial reports and regulatory submissions...
apartmentAscendis Pharma A/SplaceHeidelberglanguageappcast.ioevent_available
Would you enjoy leading drug development for rare conditions? Are you a medic with experience designing clinical trials and interacting with regulatory authorities? If so, now is your chance to join Ascendis Pharma as our new Associate Medical...
apartmentDr. Falk Pharma GmbHplaceFreiburg im Breisgaulanguagestepstone.deevent_available
key liaison between Clinical Research Gastroenterology II, Global Safety, Pre- and Early Clinical Research, and Regulatory and Medical Affairs. GL drives execution for assigned projects in collaboration with other cross-functional stakeholders. Key...
apartmentIndegeneplaceDeutschlandlanguagemindmatch.aievent_available
deceptive and misleading and is in accordance with applicable German regulatory framework and code of conduct.  •  Provide strategic input and guidance on regulatory affairs matters, including understanding the collaboration between global and local markets...
placeMünchenlanguagemedpace.comevent_available
Clinical Safety Coordinators on safety reporting responsibilities  •  Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs...

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