Deliver high-level scientific input through expert bibliographic services, including in-depth literature searches, reviews, and evidence-based analysis aligned with local Medical Affairs and Commercial strategy.
Identify, analyze, and report trends in local medical and scientific insights (including medical enquiries) to relevant stakeholders and Global Medical Information (GMI).
Assess the need to update or build scientific materials (local standard responses, local training materials etc).
Inform LEO Pharma materials, processes and business decisions.
Develop innovative high-value initiatives to support local Medical Affairs and local business activities and interaction with customers, for example launch and maintenance of the LEO Pharma MI Website and other innovative digital platforms.
Provide timely, accurate, and clear verbal and written information in response to enquiries about the Dermatology portfolio or therapy area to ensure safe and effective use.
Conduct Legal Medical Regulatory (LMR) reviews (copy approval) of local materials (Medical and Commercial) to ensure scientific accuracy and compliance.
Create and maintain Affiliate Data on File and clinical summaries for the dermatology portfolio.
Lead Medical Information booth activities at local and global congresses, providing balanced, non-promotional scientific information on LEO Pharma marketed and pipeline products to healthcare professionals and key stakeholders, and ensure all interactions are accurately logged in the Global Medical Information Database.
Contribute to the development of Global Medical Information strategy and participate in GMI projects and tasks as required.
Build strong and collaborative relationships with other global LEO Pharma Medical Information colleagues to build synergies and help drive efficiencies.
Support and assist the Affiliate Team Manager and Local Country Medical Director as required.
Qualifications
Scientific Degree level or equivalent/Pharmacist/Nurse
Significant experience in a Medical Information role in the pharmaceutical industry
Have a strong and high level of scientific knowledge to be able to analyse data from all types of clinical data including Clinical Study Reports and published data in all forms etc.
Must have proven strong technical/scientific writing skills and verbal communication including face to face with Healthcare Professionals and presenting to a variety of audiences
Proven high level technical and compliance skills when reviewing LMR materials and authoring SOPs and other high-level process driven documentation
Bilingual (French, English) preferred
In-depth knowledge and efficiency in Medical Information systems
Knowledge and experience of working in global and/or local cross functional teams
Experience in leading and managing Medical/Scientific Information Booths at Congress
High level knowledge and understanding of technical reviews within LMR frameworks