EC | HEALTHCARE

Would you like to join the European market leader and contribute to our mission to extend and improve people’s lives? If you answer is yes, then join Sandoz and our Region Europe business! Drive central value creation across the region to support the Sandoz vision of being #1 in sales and market share in the Region Europe Biosimilars & Specialty business. Your responsibilities include, but not limited to: Lead project management responsibilities for strategic marketing initiatives that cut across the entire region and function in strong collaboration with the marketing & cross-functional team, including support functions; ...

Due to its expanding portfolio, Vifor Pharma has an excellent opportunity for a Clinical Development Director for our nephrology therapy area. This role will be a part of our global clinical development team based in Glattbrugg, Zurich. Reporting to the Clinical Development Lead for nephrology, the Clinical Research Director will be responsible for medical and scientific contribution to protocols, new product and indication opportunities, drug safety, study reports, IBs, regulatory submissions, manuscripts, medical education, and other projects requiring medical/scientific research, analysis, evaluation, training and reporting. ...

Bei Rochus Mummert's Mandanten handelt es sich um ein führendes Technologieunternehmen, welches national wie international sehr erfolgreich ist. Es entwickelt, produziert und vertreibt hochwertige Medizinprodukte und ist einer der Premiumanbieter seines Marktes. Es gehört zu den führenden Markenanbieter der Branche und genießt bei Kunden sowie bei den eigenen Mitarbeitern einen hervorragenden Ruf. Ihre Aufgaben: Entwicklung und Umsetzung der Prozesse zur optimalen Abwicklung von Kundenaufträgen; Strategische Planung der Lieferketten und Optimierung der dazugehörigen Organisationsabläufe; ...

As (Associate) Director Global Commercial Programs, you will be a key member of the commercial team, coordinating all commercial activities across product development, including product launch. In this role, you will be working cross-functionally with your colleagues within Commercial as well as with the R&D program teams (incl. e.g. Clinical, Regulatory and Supply) in order to execute commercial strategy and planning for several oncology assets from BioNTech's RNA cancer vaccine platforms. ...

Ihre Aufgaben: Konzeption neuer Lösungsangebote für Kunden in Niederlassung und Klinik, aufbauend auf aktuellem Produktportfolio aber auch darüberhinausgehend; Pilotierung neuer Angebote mit dem Ziel, schnellstmöglich eine Entscheidung über Ausbau oder Aufgabe zu treffen; Evaluierung globaler und regionaler Vorschläge für eine mögliche Pilotierung bzw. Umsetzung im deutschen Markt; Entwicklung von Bezahlmodellen für neue Lösungsangebote bzw. Abschätzung eines generellen Marktmodells für Begutachtung der Attraktivität neuer Geschäftsmodelle; ...

The Associate Director, Global Regulatory Affairs Development Strategy (GRA-DS) will be responsible for developing and implementing regulatory strategy leading to successful registration and life-cycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs. This individual will, with a high sense of urgency, provide operational and strategic regulatory input to cross-functional teams responsible for global programs. The individual will also ensure effective communication and constructive working relationships with business partners and representatives of regulatory authorities. ...

The Global Medical Director will lead and contribute to the development and execution of the strategy in Amyloidosis by providing strong scientific and medical expertise with an in-depth understanding of the disease area and unmet medical needs, consistent with the GMA’s mission to maximize patient outcomes and advance the evidence-based medical standard of care. This role will require matrix leadership and broad internal cross-functional collaboration with global functions (Commercial, Clinical Development, Regulatory Affairs, etc) as well as the International Region and Japan. ...

Join us as a Director Medical, Writing for our Vaccines Business Unit, based in Zurich. Here, you will be a vital contributor to our inspiring, bold mission. Objectives: The Director, Medical Writing is responsible for strategically planning and resourcing the medical writing deliverables that support Takeda’s business objectives for clinical development for Vaccines Business Unit with multiple compounds through all phases of development. This position provides medical writing therapeutic leadership responsible for the ...

Der/Die Medical Indication Lead ist für alle lokalen medizinischen Angelegenheiten und Entwicklungsaktivitäten in den definierten Indikationsbereichen verantwortlich. Zu Ihren Verantwortlichkeiten gehören, unter anderem, die Folgenden: Eigenverantwortliches Ressourcemanagement und Priorisierung im Team, um die vorgegebenen Ziele effektiv und effizient zu erreichen. Verantwortlichkeit für die lokale Strategie der Medizin der jeweiligen Indikation, einschließlich klinischer Studien, medizinischer Kommunikation, medizinischer Ausbildung, wissenschaftlicher Projekte und wissenschaftlicher Forschung. ...

In 2020, Gilead completed the acquisition of a number of companies which are developing innovative treatments in the field of oncology. One of the leading compounds is a novel Antibody Drug Conjugate (ADC), which is being investigated for its potential application across various types of cancer. Due to the anticipated regulatory authorisation of this new ADC in 2021, an exciting opportunity has arisen for a talented and experienced marketer to join Gilead as Oncology Marketing Director in the UK & Ireland affiliate. This newly created position will be based in Holborn, London and report into the Business Unit Director. ...