Qui sommes-nous ?
Laboratoires Pierre Fabre employs more than 10 000 people in 41 countries.
The company's products can be found in all areas of the healthcare sector,
from prescription drugs and over-the-counter medicines to dermo-cosmetics.
Votre mission
Missions :
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
In addition as required:
Develop relationships and scientific partnerships with opinion leaders and treatment centers with the goal of optimising patient care and developing clinical research.- Provide scientific and medical information in response to requests from healthcare professionals and gather information intended for the medical department, specifically the Clinical Development division
- Implement international and local regulations and company rules along the processes and procedures of Clinical Development activities as needed and in line with the guidance from Global Clinical Development
- Arrange, if necessary, training or scientific support for medical representatives associated with the Clinical Development sites or medical community networks
Qui êtes-vous ?
Requirements:
- MD and/or PhD with clinical development experience
- In-depth understanding of oncology precision medicine concepts, their clinical translation and global landscape
- Experienced in planning, oversight and execution of clinical trials in oncology or experienced in clinical trial conduct in investigator sites
- Experienced in operating within matrixed global teams
Excellent and pro-active communication skills
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.
