Additional Information
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.
💊 A pharmaceutical group with a strong positioning: medical and natural
🥈 The second largest dermocosmetic laboratory in the world
🥈 The second largest French private pharmaceutical group
🥇 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:
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.
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:
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.
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:
Assist in identifying and selecting appropriate clinical trial sites, including feasibility and pre-selection visits.
Provide corporate with local insight on key elements of the study and review local documentation as needed.
Contribute to regulatory process if relevant (e.g. obtention of documents mandatory for submission to EC)
Involvement in liaising with the site on study start up activities (e.g. contract signature)
Clinical Trial conduct support:
Collaborate with cross-functional teams to support the planning, execution, and monitoring of clinical trials.
Provide training, support, and guidance to investigators and site staff, ensuring protocol adherence, patient safety, and data quality.
Participation to Site Initiation Visits and any other visit if specific need.
Cross-Functional collaboration
Participation to Corporate Clinical Trial Team
Who you are ?
Education:
Medical Doctor (MD) and/or PhD, preferably specialized in Oncology, with experience in Clinical Development.
Deep understanding of precision oncology concepts, their clinical translation, and the global oncology landscape.
Pierrefabre · Spain