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Medical Information Pharma jobs
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- Pierre FabreReading
- Scientific support to medical team and wider cross-functional team.
- Supporting the Medical Team in timely reporting; providing medical updates to internal…
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- Syneos Health Commercial SolutionsLondon
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- Vertex PharmaceuticalsPaddington
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- ICON PlcSwansea
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- Phillips MedisizeChippenham
- Discreet and trustworthy when handling confidential and sensitive information.
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- Red NucleusRemote
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- サイネオス・ヘルスLondon
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- Ipsen LtdLondon
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- Hims & HersLondon
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- PfizerWalton-on-Thames
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- Fresenius Medical CareWillebroek 2830
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- Chapter 2London EC2A 4LU
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- Promatica DigitalRemote
- You will work with our clinical safety, information governance and technical teams, build strong relationships with GP practices and PCNs, and contribute…
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- Takeda PharmaceuticalLondon
- Strengthen scientific capability across LOC medical teams by enabling aligned training, scientific exchange, and practical application of medical priorities…
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- Bio Pharma ResourcingLondon
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Job Post Details
Job details
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Reading
Full job description
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.
Qui êtes-vous ?
Nous sommes convaincus que la diversité est une source d’épanouissement, d’équilibre social et de complémentarité pour nos collaborateurs, nos offres sont donc ouvertes à toutes et tous sans restriction.
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