Clinical Development Liaison

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.

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

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.