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About the Role
The Medical Advisor - Dermocosmetics will provide medical and scientific support for all medical activities, acting as the expert voice for assigned medicinal products and therapeutic areas. This role involves creating and executing medical plans, ensuring compliance with various codes of practice, and supporting cross-functional teams.
Responsibilities
- Provide Medical / Scientific support for all Medical activities.
- Represent the Affiliate's Medical / Scientific voice of expertise for assigned Medicinal Product(s) and relevant therapeutic areas.
- Responsibility for Medical plan creation, support and execution.
- Lead the brand team with medical support to ensure compliance to CTPA, ASA, CAP, MHRA, CMA, OPSS, ABPI, IPHA and EFPIA codes of practice.
- Ensure high standards are kept at all times in relation to compliance.
- Monitor and understand relevant therapeutic areas, including clinical trial data, consumer studies, and local practice factors.
- Conduct data and competitive intelligence analysis.
- Analyze, interpret, and report from related pharmaceutical industry environments.
- Provide scientific support to the medical team and wider cross-functional team.
- Support the Medical Team in timely reporting and providing medical updates to internal stakeholders.
- Represent the UK as a point of contact for Global Medical Affairs Teams to ensure consistency of Medical strategy within the portfolio.
- Provide Medical / Scientific expert advice / guidance to key stakeholders for assigned Medicinal Products and relevant therapeutic areas.
- Develop a professional network to allow access of ideas, expertise and capabilities.
- Engage in scientific exchanges with experts through Advisory Board Meetings, Scientific & Health Education Meetings, Clinical Trials, Data Presentation and Analysis, and one-to-one and group discussions.
- Create and deliver KTL, Patient Group & National Stakeholder mapping & engagement plans.
- Conduct effective external interactions with relevant external stakeholders.
- Organize national / regional meetings, such as scientific meetings & educational programmes, symposia, and academic meetings.
- Provide Medical Affairs support to cross-functional Affiliate teams, ensuring integration and functional independence.
- Provide Medical / Scientific input into Commercial Brand plans.
- Lead on Medical Training in ITPs, building scientific capabilities of Field Teams.
- Provide cross-functional support to HEOR and Market Access Teams for HTA submissions.
- Provide cross-functional support to Clinical Operations / R. & D. for Pierre Fabre sponsored clinical studies.
- Analyze and follow up on Investigator-Initiated Study (IIS) proposals.
- Understand data gaps, available methodologies, data collection processes, and analysis required for Real-World Data (RWD) evidence generation.
- Represent Pierre Fabre at HCP Scientific Meetings and Congresses.
- Meet KOLs in person as per field activities (recommended up to 20% of time).
- Conduct all activities within local Ethics & Compliance, Medical, Regulatory and Legal frameworks, as well as within Affiliate SOPs.
Requirements
- Comprehensive and up-to-date understanding of all relevant clinical trial data and consumer studies.
- Understanding of associated local practice factors.
- Experience in data and competitive intelligence analysis.
- Ability to analyze, interpret and report from related pharmaceutical industry environments.
- Ability to provide scientific support to medical and cross-functional teams.
- Experience in providing medical updates to internal stakeholders.
- Experience representing a region for global medical affairs.
- Ability to provide Medical / Scientific expert advice / guidance to key stakeholders.
- Experience developing professional networks.
- Experience in scientific exchanges with experts.
- Experience creating and delivering KTL, Patient Group & National Stakeholder mapping & engagement plans.
- Experience in external interactions with relevant external stakeholders.
- Experience organizing national / regional meetings.
- Experience providing Medical Affairs support to cross-functional Affiliate teams.
- Experience providing Medical / Scientific input into Commercial Brand plans.
- Experience leading on Medical Training.
- Experience supporting HEOR and Market Access Teams for HTA submissions.
- Experience supporting Clinical Operations / R. & D. for sponsored clinical studies.
- Experience in Investigator-Initiated Study (IIS) proposal analysis and follow-up.
- Understanding of Real-World Data (RWD) data gaps, methodologies, collection processes, and analysis.
- Experience representing the company at HCP Scientific Meetings and Congresses.
- Ability to meet KOLs in person as per field activities (recommended up to 20% of time).
- Adherence to local Ethics & Compliance, Medical, Regulatory and Legal frameworks, as well as Affiliate SOPs.
Skills
- Medical support
- Scientific support
- Medical plan creation
- Compliance management
- Therapeutic area knowledge
- Clinical trial data analysis
- Consumer studies analysis
- Competitive intelligence
- Data interpretation
- Reporting
- Pharmacovigilance
- Cosmetovigilance
- Stakeholder engagement
- Medical strategy
- Scientific exchange
- External interaction
- Meeting organization
- Cross-functional collaboration
- Commercial brand planning
- Medical training
- HTA submissions
- Clinical study support
- Investigator-Initiated Study (IIS) analysis
- Real-World Data (RWD) analysis
- HCP engagement
Location
- UK
Work Type
- Full-time
Experience Level
- Medical Advisor
About the Company
- Pierre Fabre is a pharmaceutical and dermo cosmetics company operating within oncology and skincare.
- The company is part of a larger French-owned Group and is owned and governed by a Foundation.
- The organization is committed to improving the lives of others and takes pride in its heritage and values.
Equal Opportunity
- Diversity is a source of fulfillment, social balance and complementarity for our employees.
- Offers are open to all, without restriction.