Senior Biostatistician

Who we are

Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.

Akkodis is a global digital engineering and smart industry leader, bringing together talent and technology to engineer a smarter future. With more than 50,000 experts worldwide and over 1,000 in Belgium, we support companies across industries in innovation, digital transformation and R&D; from consulting and talent solutions to end-to-end project delivery. Driven by passion, expertise and impact, we make incredible happen.

In Belgium, we operate through 7 dedicated practices, where our consultants receive the technical guidance, coaching and support they need to grow and fully unlock their potential. We believe in empowering our talent by providing the right expertise, knowledge-sharing and development opportunities to help them thrive. Our practices: Product & System Development, Validation & Verification, Manufacturing & Operations, Cloud Infrastructures & Security, Data Analytics & Artificial Intelligence, Digital & Software and Wireless & Connectivity.

Akkodis is part of the Adecco Group. You can find more information on our website: OUR TEAM AS A:

Senior Biostatistician – Clinical Trials

Your responsibilities:

As a Senior Biostatistician, you will support clinical development activities, with a particular focus on early-phase neurology trials. You will provide statistical expertise across study design, protocol development and statistical analysis planning, while working closely with clinical and external partners.

• Contribute to the statistical design of early-phase clinical trials, ensuring appropriate and robust methodologies
• Provide statistical input into clinical trial protocols and the overall clinical development plan
• Develop and contribute to Statistical Analysis Plans (SAPs), including the definition of appropriate statistical methods and analyses
• Contribute to the preparation of statistical deliverables, including TLG shells and other study documentation
• Work closely with CRO partners to develop statistical deliverables and ensure alignment with study objectives and internal standards
• Provide internal oversight and perform quality checks of CRO statistical work and deliverables
• Ensure statistical activities are conducted in accordance with relevant scientific and regulatory guidelines
• Support multiple studies simultaneously while ensuring high-quality and timely delivery
• Collaborate with cross-functional teams and communicate statistical concepts clearly to both statistical and non-statistical stakeholders
• Contribute to the interpretation of study results and provide statistical expertise to support clinical development decisions

Your profile:

• Advanced degree (Master's or PhD) in Biostatistics, Statistics, Mathematics or a related quantitative field
• Significant experience as a Biostatistician within pharmaceutical, biotech or clinical research environments
• Proven experience supporting clinical trials, ideally including early-phase studies and/or neurology
• Strong expertise in clinical trial design and statistical methodology
• Demonstrated experience developing or reviewing Statistical Analysis Plans (SAPs) and statistical deliverables
• Experience preparing TLG shells and supporting xlxgzvr clinical study reporting
• Good understanding of international scientific and regulatory guidelines, including ICH, EMA, FDA and/or PMDA
• Experience working with CROs, including oversight and quality review of external statistical deliverables
• Strong organizational skills and ability to manage multiple studies and priorities simultaneously
• Excellent written and verbal communication skills
• Fluent in English

Location: France / Remote

Candidates based in Belgium can be considered for this remote assignment.

OUR OFFER:

As an Akkodis consultant, you will be:

• Involved in high-impact, scientifically driven projects within the pharmaceutical and life sciences industry
• Supported in your career by your dedicated Akkodis Manager
• Actor of your own training plan and professional development
• Member of a dynamic and collaborative community of engineers and scientists
• Benefiting from a permanent contract
• Benefiting from a competitive salary package including several extra-legal benefits