Description
Hays ist ein weltweit führender Personaldienstleister, der sich auf die Rekrutierung von Spezialisten konzentriert - sowohl für den Projekteinsatz als auch für Festanstellungen und auf Zeit. In Deutschland, Österreich und der Schweiz vertrauen mehr als 600 internationale Topunternehmen auf unsere qualitätsgesicherten Prozesse, wenn Sie Experten suchen.We are looking for a
International Medical Manager (m/f)
Referenz: -en
Beginn: asap
Dauer: 12 MM
Ort: in Basel region
Branche: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Providing medical input for the execution of global medical plan for the assigned product
- Implementation of Medical Affairs data generation activities (e.g. protocol and Clinical Study Report writing, data outputs)
- Communicating and collaborating closely with Clinical Trial Managers to support appropriate information flow
- Coordinating the global review of brand local clinical trial proposals
- Contributing to the development of the medical content of medical communications & medical education programmes, publications, meetings, and symposia
- Ensuring the medical review of the promotional materials for the accuracy of the information
- Ensuring the medical review of Global Publications
- Providing brand medical input to the medical information function
- Supporting the organization of internal and external meetings, events and training programs
- Supporting the organization of international medical advisory boards
- Contributing to the development of Key Opinion Leader Programs
- Organizing and leading independent data and data safety monitoring boards, and trial steering comittees
Ihre Qualifikation
- Medical, scientific, or pharmaceutical degree (ideally MD or PhD )
- Profound experience within the pharmaceutical industry (e. g. in medical function at global or country level and within area of Oncology and/or Hematology)
- Development and implementation of clinical trials
- Medical information and communication management
- Experience in writing clinical publications and relevant scientific knowledge
- Drug development process and regulatory requirements for drug registration, clinical trials and medical communication
- Fluency in written and spoken English
Skills:
- Medical Affairs