Biostatistician

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Our mission at Akkodis is clear: create a smarter future together!
We are a one-stop-shop for engineering, IT, Life Science, and new technologies.
Our combined passion for talent and technology allows us to look at the world differently.
With our 360° offer, we support companies in all sectors in implementing Smart Industry solutions, from the up- and reskilling of entire teams to the delivery of complete projects.
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Make the incredible happen! At Akkodis, you can take your career in the direction you want: choose a consulting role, become part of solutions teams, or be at the forefront of new innovations from within our own research centres… the choice is yours!
JOB DESCRIPTION : As a biostatistician, you will: Provide expert statistical input and contribute to development plans, design, protocol writing, statistical analysis, and interpretation of results from clinical studies.Ensure the timely availability of high-quality analysis results to support decision-making.Offer statistical oversight and guidance to teams and outsourcing partners.Tasks and responsibilities include: Contributing to the design, analysis, and interpretation of clinical studies, collaborating with clinical representatives, safety teams, and data management teams.Writing and reviewing key clinical and statistical documents such as Protocols, SAP, DMP, CRF, and CSR.Providing high-quality and timely statistical analyses to support decision-making.Acting as a statistical representative within cross-functional study teams and project sub-teams.Supporting interactions with health authorities and preparing relevant documents.Contributing to internal process improvements and developing new statistical capabilities.Maintaining current scientific and regulatory knowledge.Required competencies: MSC or PhD in Statistics or related field.Experience as a statistician in the pharmaceutical industry.Proficiency in English (oral and written).Good programming skills in SAS (Macro, SQL) and R.Strong knowledge of statistical methodologies applied to clinical projects.Ability to propose and implement new statistical methodologies.Excellent knowledge of GCP and ICH guidelines.Strong communication skills and ability to explain complex statistical concepts clearly.Leadership skills to lead statistical and programming teams.Ability to manage and meet delivery timelines.Team player with experience working in multidisciplinary teams.Knowledge of regulatory requirements (e.g., ICH E9/E10).Technical knowledge of CDISC standards (ADaM, SDTM).Experience with submission processes and interactions with health authorities.
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