Who we are ?
The Pierre Fabre Group, of the Pierre Fabre Foundation, is a global company with a unique position: the alliance of pharmaceutical and dermocosmetic expertise.
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💊 A pharmaceutical group with a strong positioning: medical and natural
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🥈 The second largest dermocosmetic laboratory in the world
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🥈 The second largest French private pharmaceutical group
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🥇 Market leader in France for products sold without a prescription in pharmacies.
We believe in inclusive workplaces, where the differences between people are respected, valued and cared for to develop talent in equal opportunities.
Your mission
**The Clinical Development Liaison is a Clinical Development role in the affiliate, providing medical/scientific input into the development and execution of clinical trial conducted in R&D. It acts as the Clinical Development local representative making the link between the investigators & sites and the Global Clinical Development team. The candidate should ideally be a Medical Doctor (MD), preferably Oncologist with clinical development experience. **
Local Intelligence:
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Stay updated on local landscape, latest medical and scientific developments in the relevant therapeutic area(s). Provide insights to internal teams, healthcare professionals, and investigators.
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Mapping, profiling of health care professionals / treatment center / health care organization / PAG. Deep and updated knowledge of medical (patient management according to disease, unmet needs, competitors…) and patient pathway (including testing capabilities). Identify local patient journey.
KoL Management & Sponsor representation:
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Pierre Fabre Clinical Development local representative. Presence in congress, scouting, networking. Identification of centers of interest. Presentation of PF portfolio. Provide medical/scientific input into the development and execution of clinical trial, including initiation and oversight of clinical studies within the respective therapeutic area.
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Clinical trial stakeholders Engagement: Build and maintain strong relationships with investigators and any other local stakeholder involved in clinical trials (ie. PAGs , healthcare professionals) to provide scientific support, gather insights, and facilitate collaborative research opportunities.
Study Set-up:
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Assist in identifying and selecting appropriate clinical trial sites, including feasibility and pre-selection visits.
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Provide corporate with local insight on key elements of the study and review local documentation as needed.
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Contribute to regulatory process if relevant (e.g. obtention of documents mandatory for submission to EC)
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Involvement in liaising with the site on study start up activities (e.g. contract signature)
Clinical Trial conduct support:
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Collaborate with cross-functional teams to support the planning, execution, and monitoring of clinical trials.
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Provide training, support, and guidance to investigators and site staff, ensuring protocol adherence, patient safety, and data quality.
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Participation to Site Initiation Visits and any other visit if specific need.
Cross-Functional collaboration
- Participation to Corporate Clinical Trial Team
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.