Medical Affairs Lead RIA
Baar, Switzerland
We are recruiting a Medical Affairs Lead within the therapeutic area of RIA (Respiratory, Inflammation and Autoimmunity), reporting directly into the Medical & Regulatory Affairs Director Switzerland.
In this position you have the medical lead within your assigned therapeutic area (TA) and you are managing the TA’s Medical Affairs team. You are acting as the proactive strategic partner within the Business Unit BU for medical excellence in your assigned TA. You are the bridge between the CH and the WESE/EUCAN/Global Medical Affairs organization and you are building the BU’s strategy and providing Swiss level insights for the WESE/EUCAN/Global Medical Affairs strategy
The Medical Affairs Lead RIA has people management responsibilities, leading one (or more) Medical Advisors (MAs) and Medical Science Liaisons (MSLs). The Medical Affairs Lead RIA is the scientific partner to the business, thus supporting the overall company business goals. In this role you are expected to lead changes in organizational behaviors to successfully implement a medical deployment for a specific therapeutic area in line with BU’s expectations.
Your Tasks and responsibilities
Your Profile / Qualifications / Experience
Develop and coach a high quality team
Leadership; skills and personal characteristics
Education
Language
Fluency in German and English is essential, any additional local language is a plus
We offer:
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.
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