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 healthcareprofessionals) 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 clinicaltrials.
• Provide training support and guidanceto 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

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.

Experience:

• Experience in the planning oversight and execution of oncology clinical trials is required or experience conducting clinical trials at research centers.
• Experience working within global matrix organizations.
• Excellent and proactive communication skills.

Languages:

• English C1 level required.
• French is considered an asset.

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.