Medical Affairs Stellenangebote Mainz

 ...Associate Director Regulatory Affairs Commercial Portfolio* Germany  You will be member of the Regulatory Affairs Commercial...  ...matters from e. g. Labeling (German product informative texts), Medical Affairs, Pharmacovigilance and CMC. Regulatory activities might... 

 ...medizinischen Ausbildung erfolgt in Zusammenarbeit mit dem Field Medical Director, um den Kundengruppen ein einzigartiges medizinisches...  ...Das bringen Sie mit: • Erfahrung im Bereich Medical Affairs in der pharmazeutischen Industrie, vorzugsweise in einer Rolle... 

 ...Director, Project Leader IT Implementation Medical Affairs Tasks: Manage complex technology and/or data-driven projects that include multiple workstreams and multiple stakeholder groups, and demonstrated track record of having successfully delivered... 

 ...Sr Dir Global Regulatory Affairs Development Pipeline - Portfolio Lead (Infectious Diseases)  Core responsibilities: Supervise the design and execution of Regulatory Strategy for clinical development towards global marketing authorisation across... 

 ...mit seltenen Krankheiten zu transformieren. Werde jetzt Teil unseres Teams bei Novo Nordisk!   Über die Abteilung Unser Medical Affairs Team übernimmt die medizinische und wissenschaftliche Betreuung unserer vermarkteten und in der Entwicklung befindlichen Präparate... 

 ...(Senior) Director Global Regulatory Affairs Development Pipeline - Project Lead Your purpose on this position is to lead all regulatory activities required for development of investigational medicinal products toward marketing authorisation for global markets... 

 ...Development We are looking for you to join us as (Senior-) Medical Director to help drive our cutting-edge oncology pipeline. In...  ...endpoints, synthetic control arms, RWE/HEOR, PRO, Medical Affairs). Own and ensure preparation for clinical sections of key documents... 

Über uns Where people make the difference Der Arbeitsalltag bei Midas Pharma ist abwechslungsreich und herausfordernd. Diese Herausforderung motiviert und inspiriert uns. Das spiegelt sich auch in den Menschen, die hier arbeiten: Unsere Mitarbeitenden machen den Unterschied...

Director* Non-Clinical Safety & DMPK as DMPK Team Lead  At BioNTech, you will contribute to non-clinical development and safety activities for global R&D programs and new technology platforms during different stages of pharmaceutical development by implementing...

 ...protocol and clinical study level. · Contributes to the trial medical/ safety aspects and risk-benefit assessments supported by the...  ...endpoints, synthetic control arms, RWE/ HEOR, PRO, Medical Affairs) · Creates input for clinical sections of key documents, including... 

 ...Biologe, Pharmazeut, Chemiker als Regulatory Affairs Manager - Medizinprodukte Wir suchen im Auftrag eines global agierenden Pharma- und Medizinprodukteherstellers eine*n erfahrene*n Regulatory Affairs Manager (m/w/d), der*die uns dabei unterstützt, Marktzulassungen... 

 ...Qualifikation Abgeschlossenes naturwissenschaftliches Studium z.B. Chemie, Lebensmittelchemie o.Ä. Berufserfahrung im Bereich Regulatory Affairs bzw. in der Zulassung von Bioziden Profunde Kenntnisse auf dem Gebiet der Prüfung von physikalisch-chemischen Eigenschaften und/... 

(Associate) Director* Product Quality - mRNA Oncology  (Associate) Director* of Product Quality The (Associate) Director* of Product Quality is accountable for end-to-end quality oversight of mRNA Oncology program(s) throughout clinical development, commercialization...

Das Zentrum für Allgemeinmedizin und Geriatrie sucht zum 01.05.2024 für das pflegerische Team: Pflegefachkraft (m/w/d) als Stationsleitung Wir bieten Ihnen: Gestaltungsspielraum und Entwicklungsmöglichkeiten Berufliche Weiterentwicklung in einem interessanten...

 ...This includes thorough data interpretation based on deep scientific and disease biology understanding, translational expertise and medical knowledge, including patient safety and data integrity Your main responsibilities are: Works hand-in-hand with the... 

Associate Director* Clinical Quality Assurance Compliance The Associate Director* Clinical QA Compliance supports and oversees the proactive and risk-based Quality Strategy implementation in the clinical development activities within a portfolio. ...

Specialist* R&D Program Management  We broaden the universe of patients, improving the success rate and exploiting the full potential of the immune system. Through your innovation, passion and unity with your colleagues you can become a pioneer in our Global R&...

 ...VP* Global Regulatory Affairs - Development Pipeline Your main responsibilities are: Define and establish overarching regulatory approaches across all product classes and through all development phases. Supervise and endorse global regulatory strategies...