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Medical Lead IAI Dermatology Specialist

Il y a 2 mois


BoulogneBillancourt, Île-de-France Incyte Temps plein
About the Role

We are seeking a highly skilled and experienced Therapeutic Lead Medical Affairs Specialist to join our team at Incyte Biosciences France. As a key member of our Medical Affairs Department, you will be responsible for deploying the medical strategy on the therapeutic area of expertise dedicated to Vitiligo.

Key Responsibilities
  • Develop and maintain expertise in the field of Vitiligo, staying up-to-date with the latest literature, management, disease environment, and available data on products and products under development.
  • Contribute to the realization and monitoring of medical strategic plans in the therapeutic area of interest.
  • Support the organization of medical events, such as symposia, advisory boards, and national medical meetings.
  • Provide medical and scientific contributions to related activities, including projects for patients, communication campaigns, scientific symposia, and medical meetings.
  • Support the adaptation, review, and validation of EU and/or local training and scientific materials for provision of medical teams and marketing/sales teams.
  • Participate in the proposal for French centers for Incyte-sponsored studies.
  • Follow the conduct of Incyte or academic clinical trials in the therapeutic area of interest in coordination with the EU team.
  • Accompany the establishment of scientific partnerships with the scientific community involved in Vitiligo.
  • Support the plan of collaboration and external engagement and its follow-up.
  • Contribute to internal scientific training for MSLs, KAMs, and other departments.
  • Follow the budget attached to the projects under his/her responsibility.
  • Share his/her experience with colleagues in Medical Affairs in France and Europe.
  • Represent the medical team in transverse projects in France and in Europe.
  • Ensure Pharmacovigilance monitoring on areas of interest in the medical press.
  • Ensure compliance with good clinical practices and local and international regulations in place.
  • Coordinate with the DPO.
  • Comply with the Company's procedures and ensure compliance with the conformity of the legal and regulatory guidelines that govern scientific interactions with physicians and health professionals.
Requirements
  • Diploma: Master in science (5 years min.).
  • 5 years successful experience in medical affairs of a pharmaceutical company.
  • Experience in Dermatology and knowledge about the market and the needs of healthcare professionals.
  • Good knowledge of the environment and the management of skin diseases.
  • Good knowledge of clinical research.
  • Good knowledge of the environment of medical and regulatory affairs of the pharmaceutical industry in France.
  • Excellent communication skills.
  • Good communication skills with healthcare professionals.
  • Structured approach to project management.
  • Ability to work independently and efficiently in complex and changing environments.
  • Interest for innovative approaches and digital tools.
  • Good management of priorities.
  • Good working capacity in a team and across functions.
  • Proactive, capable of initiative, force of proposal.
  • Rigor.
  • Very good level in English.
  • Excellent use of office software (Excel, Word, PowerPoint) and Outlook.
  • Ability to travel regularly, sometimes with overnight stays.