Lead Statistical Programmer- CDI -M/F

Job description

Who we are ? We are Pierre Fabre Laboratories, a global leader combining pharmaceutical expertise with dermo-cosmetics to support consumers and patients at every stage of their care journey. Our portfolio includes several medical franchises and international brands such as Eau Thermale Avène, Ducray, A-Derma, Klorane, René Furterer, and Pierre Fabre Oral Care. By joining us, you become part of a meaningful company where the human dimension is essential. You become a participant in the "We Care Movement," a movement that values excellence and innovation within passionate teams. Together, we push the boundaries of science to unite health and beauty for the benefit of all, because Every time we care for a single person, we make the whole world better. Present in 120 countries with a team of over 10,000 employees, we are proud to create a scientific and human impact, today and tomorrow! If caring is at the heart of your values, join Pierre Fabre Laboratories and become a key player in the “We Care Movement". Your mission We are currently seeking a highly skilled and experienced Lead Statistical Programmer to join our Biometry Department, part of the Data Science & Biometry Department based in Toulouse (31, Langlade, Oncopole) or Boulogne (92). This position requires a strong expertise in the application of programming within the context of randomized controlled trials (RCTs). The successful candidate will be agile and adaptable, capable of working in a matrix-organized environment where collaboration across Data Management, Programming, and Statistics is essential. Whilst an excellent track record in Randomized Controlled Trials is a must, the successful candidate will also contribute to Real Worl Evidence (RWE) studies. Your role within a pioneering company in full expansion: Key Responsibilities Participate in the design and execution of RCTs and RWE studies, ensuring high-quality programming support. Develop and validate programs for data analysis, reporting, and visualization in accordance with regulatory guidelines and standards (e.g., ICH, EMA, FDA, PMDA). Collaborate with statisticians, data managers, and other stakeholders to ensure accurate and efficient data processing and analysis. Assist in the selection and evaluation of subcontractors, establishing clear requirements and evaluating proposals. Contribute to the preparation of regulatory documents and scientific publications by providing programming support and expertise. Follow all industry standards, including ensuring that all biometry-related documentation is included in the electronic Trial Master File (eTMF). This position is compatible with teleworking up to 2 days a week according to company rules. We offer an attractive remuneration/benefits package: Incentives, profit-sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation, very attractive CE... Who you are ? Your skills at the service of innovative projects: Advanced degree in Statistics (Master's Degree, ENSAI, ISUP, or PhD) or a related field. A minimum of 6 years of experience in the pharmaceutical industry or a Contract Research Organization (CRO), with hands-on experience in RCTs and RWE studies. Programming in CDISC (SDTM & ADaM) and writing associated documentation (Define, ADRG...) Mandatory Skills Proficiency in SAS and R programming languages Extensive experience in Randomized Controlled Trials (RCTs) Strong knowledge in CDISC (SDTM & ADaM) and associated documents (Define, ADRG, ...) Strong knowledge of international scientific and regulatory recommendations (e.g., ICH, EMA, FDA) Ability to collaborate effectively with statisticians, data managers, and other stakeholders Excellent written and verbal communication skills in English Excellent communication and cooperation skills, with a rigorous and pragmatic approach. Creativity, proactivity, rigor, autonomy, and collaborative spirit. Strong ability to manage multiple studies simultaneously and maintain organization. Optional Skills Experience with other statistical programming languages (e.g., Python, SQL) Knowledge of Real-World Evidence (RWE) studies Experience in EMA, FDA or PMDA submissions Experience in oncology clinical trials Application Process Interested candidates should submit their resume and a cover letter detailing their experience and qualifications for this position. The hiring manager is Romain Raymond , Programming & Biometry Platform Manager. The Head of the Biometry Department is Guillaume Desachy. We look forward to welcoming a new member to our dedicated and innovative team at Pierre Fabre. At Pierre Fabre Laboratories, we believe that our greatest asset is our people. We are committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee based on race, color, religion, creed, national origin or ancestry, sex, sexual orientation, gender identity or expression, age, physical or mental disability, veteran or military status, genetic information, or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identify, and maintain employment statistics on applicants. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. Please inform the company’s personnel representative if you need assistance completing this application or to otherwise participate in the application process. Thus, we commit to considering all applications equally, without fail.