European Senior Medical Advisor- Prolia
Amgen Inc.
Zug, Switzerland
vor 33 Tg.

Amgen is one of the world's leading independent biotechnology companies. For more than 35 years, Amgen has pioneered biotechnology breakthroughs, to bring state-

of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world.

We are currently seeking a European Senior Medical Advisor- Prolia for our EU Medical Organization located in Zug, Switzerland.

The primary focus of the successful candidate will be to support data generation including partnering with country teams to support investigator sponsored study implementation.

Additional objectives of this role are to support the implementation of EU medical strategies, including disease state and product related programs and partner with country Amgen medical affairs staff to develop and maintain relationships with scientific experts and various external parties.

Additional responsibilities include :

Provide EU-focused clinical input to and review of EU commercial plans and global strategic documents

Design and execute phase 4 clinical trials and observational research to support clinical and commercial activities in partnership with Development Operations, Center for Observational Research and Global Health Economics

Review EU Non-Amgen Sponsored Clinical Research (NASCR) proposals

Provide clinical input and support for publications, training, RML support, congress activities and other scientific affairs activities

Provide clinical input, review and participate in approval of materials used by medical affairs or the EU commercial organization

Provide clinical content expertise for documents and participate in meetings in support of regulatory, safety, health economic and reimbursement interactions in the EU

Assist in the execution of Advisory Board Meetings

Provide interpretation of clinical study data

Review scientific literature

Review EU donation, and sponsorship requests

Engage with key scientific experts and other important external stakeholders

Basic Qualifications : Medical Doctor or PhD degree

Medical Doctor or PhD degree

2 or more years of medical affairs and / or clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical) or significant interest in one or more of the following therapeutic areas : osteoporosis, endocrinology, rheumatology

Familiarity with national and / or EU regulatory and national access systems

Experience with scientific expert interactions incl. existence of a network

Fluency in English, both oral and written communications

Preferred Qualifications : Medical Doctor

Medical Doctor

4 or more years of medical affairs and / or clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical) in one of the following therapeutic areas : osteoporosis, endocrinology, rheumatology

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