ALSI - Respiratory Medical Affairs Director HF

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Air Liquide
Bagneux
EUR 80 000 - 120 000
Faites partie des premiers candidats.
Hier
Description du poste

Within the framework of Air Liquide Healthcare World Business Line (WBL) and reporting to the VP Market Access and Evidence, the Medical Affairs Director will contribute to achieving the company's objectives by creating the Medical Affairs Plan to support the deployment of Air Liquide Healthcare WBL programs and offers in the respiratory therapeutic areas.

The Medical Affairs Director will provide medical and scientific expertise on new projects, lead engagement with external medical and scientific communities, and coordinate the dissemination of scientific communications externally.

Medical Expertise & Education:

  • Develop and maintain scientific and medical expertise.
  • Provide disease state education, clinical presentations, and respond to medical requests.
  • Offer medical expertise on new key WBL projects, including new product/offer definitions and development.

KOL & Scientific Community Engagement:

  • Lead relationships with the medical and scientific community, particularly with global and regional medical societies, professional organizations, opinion leaders (OLs), and healthcare providers.
  • Create OL mapping and engagement plans; update internal stakeholders about interactions.

Evidence Generation:

  • Identify opportunities for strategic development through activities such as literature screening, scientific events, opinion leader networks, advisory boards, and expert panels.
  • Contribute to the Evidence Generation Plan and support clinical research, study design, setup, management of expert panels, and assessment of scientific results.
  • Attend scientific meetings and conferences, supporting the development of key data summaries and symposiums.

Material Creation:

  • Provide medical and scientific content for foundational, marketing, and communication materials.
  • Review and approve promotional and communication materials for engagement with the scientific and medical community.

Clinical Support to Regulatory Affairs:

  • Support regulatory activities with clinical expertise for market authorization, renewals, and pharmacovigilance.
  • Ensure compliance with applicable laws, regulations, guidelines, and company policies.
  • Manage medical information.

Qualifications:

  • Doctoral degree (MD, PharmD, or PhD).
  • Deep knowledge in respiratory diseases.
  • Experience in engaging with KOLs, HCPs, or the medical community.
  • Excellent communication skills in English.
  • Strong leadership qualities.
  • Leadership through vision and values.
  • Science-based approach with problem-solving attitude.
  • Results-oriented with a collaborative mindset.

Required Experience and Key Skills:

  • Experience as a Director.
  • Skills in EMR Systems, Clinical Research, Managed Care, Clinical Trials, Leadership, and more.
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