About the company.
927 million. That’s how many lives our Novartis group products touched in 2017. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this : how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment.
Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks.
And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
We are Sandoz, a Novartis Division. Join us and help reimagine medicine.
About the role.
Inform patients, Health Care Professionals (HCPs) and other external partners as well as internal stakeholders on medical, pharmacological and pharmaceutical areas in an understandable, scientific and compliant manner.
Ensure patients and healthcare providers can access all the practical and clinically relevant information in an understandable way to use Sandoz’s medicines efficiently and safely.
Your responsibilities include, but not limited to :
Responsible for in- and external advice and provision of information regarding medicines of Sandoz and related therapeutic areas, including :
Answer written and oral questions on medical, pharmacological and pharmaceutical topics from physicians, pharmacists, patients and other relations as well as from local Sandoz teams (e.
g. sales, marketing, medical, regulatory affairs);
Involve global functions to obtain additional information, if relevant;
Involve local teams (e.g. regulatory affairs or market access) to collaborate on answering inquiries;
Discuss the information gathered with the respective departments and implement adaptations in communication and information (printed and digital), if relevant.
Responsible for inventory, interpretation and availability of information by :
Identifying notifications of adverse events and pharmaceutical complaints and report them to the relevant departments;
Capture information regarding inquiries, questions and answers in a database;
Recognize trends in the inquiries, take action if necessary and inform relevant departments. Participate in (cross-functional) projects to emphasize the focus of Sandoz on patients and customers.
Report on e.g. key performance indicators according to agreed timelines.
Responsible for the process of creating shortened product information in collaboration with the regulatory affairs and marketing teams.
Develop medical plans for appointed therapeutic areas in collaboration with cross-functional teams. Execution of the approved medical plans according to agreed timelines.
Preferably a masters degree with a strong interest in pharmacology, pharmacist
Fluent in English and Dutch (verbal and written).
Between 0-2 years working experience in a pharmaceutical environment in Medical Information,
Medical Affairs or Regulatory Affairs Clinical, scientific and regulatory knowledge of the relevant therapeutic areas
Comprehensive understanding of compliance topics (e.g. GDPR, CGR guidelines)
Excellent communication and presentation skills and ability to convey messages in an authentic and convincing manner.