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Are you a savvy networker with a profound scientific background? Are looking for a role where you can shape a new and upcoming area? In this role, you will work on regulators, Health Care Professionals (HCPs) and payers education programs to pave the future for Nanomedicines. Reporting to the Nanomedicines Lead, your tasks and responsibilities will include, but are not limited to, the following:

• Maintain close relations with the regulatory network, geauthorities, academics and key opinion leaders (KOLs)
  


• Contribute scientifically to the discussion among the stakeholders in drug regulation to define, establish and harmonise appropriate regulatory standards for nanomedicines for patient’s safety and benefit
  


• Engage in the education of hospital pharmacists in collaboration with relevant institutions or organisations and internally in relevant cross-functional teams, to increase awareness and understanding of these products, of their regulations and their appropriate medical use
  


• Take advantage of the specific knowledge and experience from the Vifor Pharma product portfolio and their follow-on products
  


• Develop and shape regulatory strategies with the relevant functions, using science-based insights and principles

You hold an M.D. degree or a PhD in a Life Sciences field in addition to the following experience:

• 10-12 years’ experience in professional roles relevant to the pharmaceutical industry
  


• Credible and wide-ranging (scientific) network to get access and also acceptance by (regulatory) scientists, payers and hospital pharmacists
  


• Demonstrated experience and leadership providing scientific input to development of health care products and their use in the clinical environment
  


• Solid knowledge of the global scientific and regulatory environment
  


• Continuous training on relevant topics to keep professional and scientific qualification
  


• Flexible and result-oriented; detail conscious and precise in adopting and creating relevant standards
  good understanding of US and EU pharmaceutical market and regulations
  


• 20 to 30% travel commitment

You are a seasoned professional with the ability understand and engage in high-level, complex scientific exchange about complex concepts to establish new scientific and regulatory insights and standards. You bring outstanding interpersonal skills, enabling you to build and broaden your network internally in a cross-functional environment and externally with authorities, academics and KOLs. You apply entrepreneurial thinking and spirit. You work as a role model for others in line with the Vifor Pharma values.

Über uns

Die Vifor Pharma Gruppe – die frühere Galenica Gruppe – ist ein globales Spezialitäten-Pharmaunternehmen, das eigene Pharmaprodukte erforscht, entwickelt, herstellt und vertreibt und ein bevorzugter Partner für innovative patientenorientierte Lösungen ist. Das Unternehmen hat sich zum Ziel gesetzt, ein globaler Marktführer in den Bereichen Eisenmangel, Nephrologie und kardiorenale Therapien zu sein und weltweit Patienten mit schweren und chronischen Erkrankungen zu einem besseren Leben in Gesundheit zu verhelfen. Die Vifor Pharma Gruppe verfügt über Produktionsstätten in der Schweiz und in Portugal sowie über ein dynamisches Netzwerk von Vertriebsgesellschaften und Partnern zur weltweiten Marktabdeckung. Das Unternehmen treibt die Expansion seiner weltweiten Präsenz laufend voran, bleibt dabei aber in seinem schweizerischen Heimmarkt fest verwurzelt.

Die Vifor Pharma Gruppe besteht aus Vifor Pharma, Vifor Fresenius Medical Care Renal Pharma, ihrem gemeinsamen Unternehmen mit Fresenius Medical Care, Relypsa und OM Pharma.

Für mehr Informationen gehen Sie bitte auf: www.viforpharma.com/de/ueber-vifor-pharma/wer-wir-sind

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