Data Scientist jobs in France

Pierre Fabre is the 2nd largest dermocosmetics laboratory in the world, the 2nd largest private French pharmaceutical group, and the market leader in France for OTC products sold in pharmacies.

Its portfolio includes several medical franchises and international brands such as Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, Ren, Furterer, A-Derma, Naturactive, and Pierre Fabre Oral Care.

Established in the Occitanie region, with over 95% of its products manufactured in France, the Group employs approximately 10,000 people worldwide. Its products are distributed in about 130 countries. 86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, with a smaller share owned by employees through an employee stock ownership plan.

In 2019, Ecocert Environment assessed the Group's corporate social and environmental responsibility in accordance with ISO 26000 and awarded it the Excellence level.

Pierre Fabre was recognized as one of the World's Best Employers in 2021 by Forbes, ranking in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.

The Pierre Fabre R&D Medical Care division is hiring a Clinical Scientist to join the Clinical Development Department.

The position will be based in Toulouse (preferentially) or Boulogne, with flexible options for commuting from France/Europe and home office.

• Strategic Contributions: Collaborate with the Clinical Development Director to synthesize literature, preclinical data, regulatory guidance, and clinical insights to build program rationale. Support proposals at advisory boards, investigator meetings, and site initiations. Stay up-to-date with the clinical landscape by attending scientific and clinical conferences.
• Clinical Study Support: Contribute to study design and develop clinical documents such as protocols, investigator brochures, informed consent forms, study manuals, and clinical study reports. Work closely with CDDs and Clinical Operations to address protocol questions from authorities and ethics committees. Conduct regular clinical/medical data reviews under supervision. Participate in clinical site and vendor selection.
• Operational Excellence: Assist in organizing clinical meetings (e.g., advisory boards, data safety monitoring boards, steering committees). Engage with Clinical Operations for site startup, engagement, and recruitment. Support medical monitoring activities and data quality reviews.
• Cross-Functional Collaboration: Act as a task force leader for best practices or special initiatives. Represent the core team at governance reviews and present on special topics.

We offer an attractive remuneration and benefits package, including incentives, profit sharing, Pierre Fabre shareholding with matching contributions, health and provident insurance, 16 days of RTT holidays in addition to 25 personal holidays, public transport participation, and other benefits.

Profile: Doctor in Medicine, scientific PhD with a specialty in clinical development or research nurse or pharmacist. You possess in-depth knowledge of oncology, precision medicine, and experience in clinical protocol development, study conduct, and data oversight. Knowledge of GCP and regulatory requirements for oncology trials is essential.

We believe diversity fosters fulfillment, social balance, and complementarity among our employees, and our offers are open to all without restriction.

Laboratory Experience, Immunoassays, Machine Learning, Biochemistry, Assays, Research Experience, Spectroscopy, Research & Development, cGMP, Cell Culture, Molecular Biology, Data Analysis Skills

Employment Type: Full-Time

Experience: Years

Vacancy: 1