Drug Regulatory Affairs Jobs in Rheinland-Pfalz
1 - 7 von 7
Suchergebnisse - Drug Regulatory Affairs Jobs in Rheinland-Pfalz
Allergan-Ludwigshafen am Rhein
project implementation via roles on the CMC Team or other cross-functional product sub-teams as needed to proactively avoid, manage, or address quality-related issues
• Collaborate cross-functionally (e.g., with Dev Sci, Dev Ops, Regulatory Affairs...
appcast.io -
Boehringer Ingelheim-Ingelheim am Rhein
ideally holding a Master's or Doctoral Degree. Additional certifications such as Specialized Pharmacist, Master of Drug Regulatory Affairs, or RAC are highly desirable.
• In-depth knowledge of Regulatory Affairs across multiple regions, including the US...
myability.jobs -
Boehringer Ingelheim-Ingelheim am Rhein
the chance to work on a variety of products, either in clinical development or post-marketing drug safety. We're particularly
interested in physicians with expertise in Mental Disorders or Retinal Diseases. If you're ready to take on this challenge...
myability.jobs -
Boehringer Ingelheim-Ingelheim am Rhein
the chance to work on a variety of products, either in clinical development or post-marketing drug safety. We're particularly interested in physicians with expertise in Inflammatory Diseases, Dermatology, Gastroenterology, Rheumatology or Pulmonology...
myability.jobs -
Boehringer Ingelheim-Ingelheim am Rhein
Epidemiology and Medical Affairs to develop safety-focused post-authorisation studies.
• Interpret clinical trial safety data for clinical trial reports and submission documents
• Review and provide medical-scientific input to regulatory documents (e.g. IBs...
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Boehringer Ingelheim-Ingelheim am Rhein
Global Epidemiology and Medical Affairs to develop safety-focused post-authorization studies
• Interpret clinical trial safety data for clinical trial reports and submission documents
• Review and provide medical-scientific input to regulatory documents...
myability.jobs -
Boehringer Ingelheim-Ingelheim am Rhein
transition milestones.
• Envision yourself at the helm of a cross-functional evidence team, integrating the output of various departments like Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance, Regulatory, Medical Affairs, Market...
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