Medical Advisor

Pierre Fabre; Reading; Hybrid; GBP 70,000 - 110,000; Full time

Job summary

Pierre Fabre UK is seeking a Medical Advisor for Dermocosmetics to provide Medical / Scientific support across activities under the Medical Director. The role requires leading medical plan development, ensuring compliance with relevant codes, and representing the medical voice for the portfolio.

The position involves collaboration with cross-functional teams, engagement with external stakeholders, and delivery of medical updates to leadership and affiliates. Based in Reading, UK, on-site role.

Qualifications

• Provide Medical / Scientific support for all Medical activities under Medical Director
• Represent the Affiliate's Medical / Scientific voice for assigned products and therapeutic areas
• Ensure compliance with industry codes of practice (CTPA, ASA, CAP, MHRA, CMA, OPSS, ABPI, IPHA, EFPIA)

Responsibilities

• Provide Medical / Scientific input into Medical plans and execution
• Lead medical training with field teams and cross-functional support to HEOR and Market Access
• Coordinate scientific exchanges with experts and engagement with stakeholders

Skills

Medical support

Scientific expertise

Regulatory compliance

Cross-functional collaboration

Job description

## Medical AdvisorPostuler: Royaume Uni - Reading: Temps plein: Offre publiée aujourd'hui: JR114511# Qui sommes-nous ?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.# Votre 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.