EU Central Medical Science Liaison – Netherlands
Viatris
Mylan Healthcare B.V.At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at every stage of life.We do so via:Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.The Role & What You Will Be DoingEvery day, we rise to the challenge to make a difference and here’s how the EU Central Medical Science Liaison role will make an impact:Conduct international Site Visits:
Establish regular site visits to build relationships with trial site management. Adhere to local regulations and maintain strict compliance.Communication with KOLs/HCPs across national borders:
Engage in accurate, scientific, evidence-based, and non-promotional communication.Respond to Medical Requests:
Provide timely and accurate responses to unsolicited medical inquiries from HCPs and external stakeholders.Identify Educational Needs:
Assess and communicate the unmet medical education needs of KOLs/HCPs within the organization.Insight Reporting:
Develop and share internal reports on Ad Board meetings, congresses, and customer insights.Support Clinical Studies:
Support investigators and sites for clinical studies.
Establish regular site visits to build trustful relationships with trial site management.
Facilitate and lead scientific discussions at investigator meetings and organize external roundtables, ad-boards, and steering committees.Lead Scientific Discussions:
Facilitate and lead scientific discussions at investigator meetings and organize external roundtables, ad-boards, and steering committees.Engage Patient Advocacy Groups (PAGs):
Collaborate with PAGs to integrate patient perspectives into clinical trials.Education and Engagement:
Develop educational materials to raise awareness.Medical Affairs Booths:
Set up and staff Medical Affairs booths at congresses, using digital tools to engage in clinical and medical discussions.Conduct RWE/HEOR Studies:
Ensure representation of diverse patient populations and consider health equity in RWE and HEOR studies.About Your Skills & ExperienceFor this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:Educational and Professional Background:
A strong commitment to the principles of Diversity, Equity, and Inclusion (DEI).
Self-motivated, adaptable to dynamic environments, with a strong sense of integrity.Commitment to DEI:
Strong affinity for digital tools and platforms, with the ability to leverage technology effectively in communications, data analysis, and project management.Personal Attributes:
Demonstrates flexibility and adaptability in a dynamic environment, with a willingness to travel as required by the role.Digital Affinity:
Strategic thinker with the ability to prioritize and navigate complex business situations. Capable of setting and achieving challenging goals independently and within a team.Flexibility and Travel:
Ability to actively listen and extract valuable insights from stakeholders, both directly and indirectly, and apply these insights strategically for the benefit of the organization.Strategic and Adaptive Thinking:
Excellent analytical and organizational skills for managing, interpreting, and presenting clinical data.Insight and Goal-Oriented:
Strong capability to read, interpret, and analyze complex research documents. Skilled in writing scientific reports and technical correspondence, with the ability to work with executives and communicate abstract concepts to both internal and external high-level audiences.
Nederland
Thu, 05 Sep 2024 01:44:29 GMT
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