Your mission
Executive Director, Clinical Development Liaison
At Pierre Fabre Pharmaceuticals Inc. our mission is to deliver breakthrough therapies in oncology and rare diseases to patient populations with high unmet needs and limited treatment options. Our belief is that every time we care for a single person, we make the whole world better. We are the US pharmaceutical subsidiary of Pierre Fabre Laboratories Worldwide, a foundation-owned company with 7 decades of impact. Pierre Fabre Laboratories is a truly global healthcare company, established in 43 countries, with products distributed in 119 territories across the globe. Pierre Fabre's foundation ownership enhances our ability to focus on creating long-term value for patients.
Building on the legacy of Pierre Fabre Laboratories, innovation is our life blood and patient experience drives everything we do. We aspire to design and develop therapeutic solutions inspired by patients and healthcare professionals; draw on science and nature as perpetual sources of inspiration; develop long-term partnerships with researchers and innovators worldwide; and place pharmaceutical ethics and climate transition at the heart of our action.
Pierre Fabre Pharmaceuticals is headquartered in Parsippany, NJ alongside Pierre Fabre USA Inc., a Pierre Fabre Laboratories subsidiary focused on dermatology and cosmetics.
SUMMARY:
The Clinical Development Liaison is a key member of the Global Clinical Development Team, based in the US. It will provide medical/scientific input into the development and execution strategy of R&D Studies conducted in US. The Clinical Development Liaison will act as the local R&D 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.
ESSENTIAL FUNCTIONS:
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 including Field Medical Directors 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
- Collaborate with HQ Field Medical Team
REQUIRED EDUCATION AND EXPERIENCE:
- 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 and local medical affairs team
- Excellent and pro-active communication skills
WORK ENVIRONMENT:
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
LOCATION: US, remote
Benefits of being a Pierre Fabre Employee
Join Pierre Fabre for competitive benefits including three medical plans, dental and vision coverage, voluntary benefits, a 401(k) plan, and more! Our offerings also include a hybrid work policy, a generous PTO policy and company holidays, paid parental leave, discounts on our products, learning and development opportunities, and access to mental health and wellness programs, creating a well-rounded work experience for our employees.
Pierre Fabre
Pierre Fabre has been recognized by Forbes as one of the "World's Best Employers" for the 3rd year running.
https://www.pierre-fabre.com/en-us
Pierre Fabre is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
Who you are ?
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.
United States
