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 the achievement of the company's objective 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 the engagement with the external medical and scientific communities, and coordinate the dissemination of scientific communications externally.
Medical expertise & education:
Develops and maintains scientific and medical expertise
Provides Disease State Education, clinical presentations and responds to medical requests.
Provides medical expertise on new key WBL projects, new product / offers definition and development.
KOL & Scientific community engagement:
Leads the relationship with the medical and scientific community, in particular with the Global and Regional Medical Societies and professional organisations, opinion leaders (OLs) and healthcare providers.
Creates the OLs mapping and engagement plan and updates the internal stakeholders about the medical community interactions.
Evidence generation:
Identifies opportunities for strategic development through active medical intelligence activities such as literature screening, scientific events and conferences, Opinion Leaders network, scientific advisory boards and expert panels and others as appropriate.
Contributes to the creation and execution of the Evidence Generation Plan and supports the company sponsored clinical research and investigation studies (evidence needs, study design, study execution, set up and management of expert panels and advisory boards, assesses scientific results).
Attends relevant scientific meetings and conferences and supports the development of summaries of key data, presentations or symposium.
Creates the medical and scientific communication plan for each of the programs under his/her responsibility, including advisory boards, congress symposia, hospital meetings and speaker programs, disease state related academies.
Material creation
Provides medical and scientific content to support the creation of the foundation marketing and communication materials.
Reviews and approves the promotional, marketing and communication materials intended to be used to engage with the scientific and medical community.
Clinical support to regulatory affairs
Supports Regulatory Affairs activities with clinical expertise for Market Authorization applications and renewals as well as for Pharmacovigilance activities.
Ensures compliance with applicable local and global laws, regulations, guidelines and company policies and procedures.
Is in charge of medical information.
Background - Experience required
Doctoral level degree (MD, PharmD or PhD).
Deep therapy area knowledge in the defined program disease area.
Demonstrated experience in KOL, HCP or medical community engagement.
Excellent oral and written communication skills in English.
Strong leadership capabilities.
Leads through vision and values.
Science based.
Problem solving attitude.
Results oriented.
Cross-functional collaborative approach.
Obtenez un examen gratuit et confidentiel de votre CV.
Sélectionnez le fichier ou faites-le glisser pour le déposer