Clinical Development Liaison Innovative Oncology DACH

Who we are?

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.

Your mission

Missions:

Local Intelligence:

1. 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.
2. 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:

1. 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.
2. Clinical trial stakeholders Engagement: Build and maintain strong relationships with investigators and any other local stakeholder involved in clinical trials (i.e., PAGs, healthcare professionals) to provide scientific support, gather insights, and facilitate collaborative research opportunities.

Study Set-up:

1. Assist in identifying and selecting appropriate clinical trial sites, including feasibility and pre-selection visits.
2. Provide corporate with local insight on key elements of the study and review local documentation as needed.
3. Contribute to regulatory process if relevant (e.g., obtention of documents mandatory for submission to EC).
4. Involvement in liaising with the site on study start-up activities (e.g., contract signature).

Clinical Trial conduct support:

1. Collaborate with cross-functional teams to support the planning, execution, and monitoring of clinical trials.
2. Provide training, support, and guidance to investigators and site staff, ensuring protocol adherence, patient safety, and data quality.
3. Participation in Site Initiation Visits and any other visit if specific need arises.

Cross-Functional collaboration:

1. Participation in Corporate Clinical Trial Team.

In addition as required:

1. Develop relationships and scientific partnerships with opinion leaders and treatment centers with the goal of optimizing patient care and developing clinical research.
2. 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.
3. 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.
4. Arrange, if necessary, training or scientific support for medical representatives associated with the Clinical Development sites or medical community networks.

Who you are?

Requirements:

1. MD and/or PhD with clinical development experience.
2. In-depth understanding of oncology precision medicine concepts, their clinical translation and global landscape.
3. Experienced in planning, oversight, and execution of clinical trials in oncology or experienced in clinical trial conduct in investigator sites.
4. Experienced in operating within matrixed global teams.
5. Excellent and pro-active communication skills.

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.