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Director of Medical Evidence Strategy (m/f) IDM Alemania
- Ref: 2180015
- Hace 9 horas
Jornada sin especificar - Contrato sin especificar - Retribución sin especificar - No se requiere experiencia
Working together for a healthier
world Founded in 1849, Pfizer
is the world's premier biopharmaceutical
company taking new approaches to better
health. We discover, develop, manufacture and
deliver quality, safe and effective
prescription medicines to treat and help
prevent disease for people. We also partner
with healthcare providers, governments and
local communities around the world to expand
access to our medicines and to provide better
quality health care and health system support.
colleagues in more than 90 countries work
every day to help people stay happier and
healthier longer and to reduce the human and
economic burden of disease worldwide.
Director of Medical Evidence Strategy (m/f) IDM
A career at Pfizer offers opportunity, ownership and impact.
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Right now, we are seeking highly qualified candidates to fill the position located virtual/Berlin prefered:
Director of Medical Evidence Strategy (m/f) International Developed Markets (IDM)
In addition to its traditional and highly cross-functional role to support the introduction and application of our medicines, the scope of regional medical affairs is rapidly evolving into an essential function to inform Pfizer's research strategy via formalized input into asset strategic plans and to contribute to our medicine's life-cycles, e.g. via scientific discussion of IIR-Proposals. Recently, regional medical affairs assumed additional responsibility on opportunities to enhance the drug label according to regional needs through planning and execution of Clinical Research Collaborations (CRCs). In the future, the evaluation and collection of real-world evidence - in collaboration with other internal and external stakeholders - will be another essential task for our group. Ultimately, a key role of medical is to analyze and translate the needs of healthcare providers/systems and to communicate the value of our medicines through clinical concepts and evidence. To succeed in today's oncology research, it is essential to have a clear evidence strategy in a highly dynamic, increasingly complex, and competitive environment.
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