Medical Advisor
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Before you apply
LocationUK - London
Typefull-time
SenioritySenior
DepartmentMedical
Company size10,000+ people
PostedOct 27, 2026 · 1w ago
Verified live3d ago
At a glanceSummarised by Seekless from the posting.
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
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)
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
Who we are ?
A unique business, Pierre Fabre in the UK is a pharmaceutical and dermo cosmetics company, operating within oncology and skincare.
Part of a much larger French-owned Group, and owned and governed by a Foundation, we are committed to improving the lives of others and take great pride in the heritage and values of the organisation.
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.
Who you are ?
We are convinced that diversity is a source of fulfillment, social balance and complementarity for our employees, which is why our offers are open to all, without restriction.