Medical Advisor

Pierre Fabre Group; England; On-site; GBP 70,000 - 90,000; Full time

Job summary

Pierre Fabre Group in the United Kingdom seeks a Medical Advisor to provide Medical and Scientific support within a dermocosmetics portfolio. The role involves leading medical plans, ensuring compliance with industry codes, and coordinating with global medical affairs and cross-functional teams to support strategy and execution.

The successful candidate will monitor clinical data, engage with external experts, and contribute to education programmes while maintaining high ethical and regulatory

Responsibilities

• Provide Medical/Scientific support for all Medical activities under the Medical Director's direction.
• Represent the Affiliate's Medical/Scientific voice of expertise for assigned Medicinal Product(s) and therapeutic areas.
• Lead Medical plan creation, support and execution.
• Ensure compliance with CTPA, ASA, CAP, MHRA, CMA, OPSS, ABPI, IPHA and EFPIA codes of practice.
• Maintain high standards of compliance at all times.
• Monitor relevant therapeutic areas and stay up-to-date with clinical trial data and consumer studies.
• Provide medical updates to internal stakeholders (Leadership Team, Global Medical Affairs, etc.).
• Represent Pierre Fabre UK to ensure consistency of Medical strategy within portfolio.
• Deliver Medical Training within ITPs and build scientific capabilities of Field Teams.
• Support HEOR and Market Access Teams for HTA submissions and cross-functional activities.
• Support cross-functional Clinical Operations/R&D for Pierre Fabre sponsored studies.
• Engage in Investigator-Initiated Study analysis and follow-up; understand Real-World Data gaps and methodologies.

Job description

Your mission

Medical Advisor - Dermocosmetics

Roles & Responsibilities

• To provide Medical / Scientific support for all Medical activities, under the overall direction of the Medical Director
• 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
• Responsibility on leading 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.
• Monitoring and understanding of the relevant therapeutic areas, including:
• Comprehensive and up-to-date understanding of all relevant clinical trial data and consumer studies, as well as the associated local practice factors
• Data and competitive intelligence analysis
• Analysis, interpretation and reporting from related pharmaceutical industry environments (regulatory, market access, pharmacovigilance, cosmetovigilance, etc…), as well as providing support to these relevant teams,
• Scientific support to medical team and wider cross-functional team.
• Supporting the Medical Team in timely reporting; providing medical updates to internal stakeholders (Leadership Team, Global Medical Affairs, etc….)
• Representing UK: a point of contact for Global Medical Affairs Teams to ensure consistency of Medical strategy within portfolio.
• Provide Medical / Scientific expert advice / guidance to key stakeholders for assigned Medicinal Products and relevant therapeutic areas; developing a professional network to allow access of ideas, expertise and capabilities
• Scientific exchanges with experts (Advisory Board Meetings, Scientific & Health Education Meetings, Clinical Trials, Data Presentation and Analysis, one-to-one and group discussions, etc…),
• Creating and delivering KTL, Patient Group & National Stakeholder mapping & engagement plans
• Effective external interactions with relevant external stakeholders (payors, PAGs, ORDMs, etc…)
• Organisation of national / regional meetings, such as scientific meetings & educational programmes, symposia, academic meetings, etc….
• Provision of Medical Affairs support to cross-functional Affiliate teams; ensuring that the Medical Affairs role is fully integrated to support the strategy and execution of Affiliate business, while being functionally independent
• Providing Medical / Scientific input into Commercial Brand plans
• Lead on Medical Training in ITPs; building on scientific capabilities of Field Teams
• Cross-functional support to HEOR and Market Access Teams for HTA submissions
• Cross-functional support to Clinical Operations / R. & D. for Pierre Fabre sponsored clinical studies
• Clinical Research Activities: Investigator-Initiated Study (IIS) proposal analysis and follow-up
• Real-World Data (RWD): Understanding the data gaps, available methodologies, data collection processes and the analysis required for evidence generation .
• Representing Pierre Fabre at HCP Scientific Meetings and Congresses
• Meeting KOLs in person as per field activities (recommended up to 20% of time).
• All these activities are conducted within local Ethics & Compliance, Medical, Regulatory and Legal frameworks, as well as within Affiliate SOPs.

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