Biostatistician (AD - Director Level)
reputed company are currently partnered with an innovative Biotechnology company advancing a portfolio of early- and late-phase Oncology programmes. They are urgently seeking a Senior Statistical Consultant / Associate Director (Biostatistics), reporting to the Senior Director Biostatistics, to support their expanding Biometrics team. The role will focus on providing strategic and hands-on statistical leadership across reputed company oncology studies, including early-phase trial design. See a summary of the role below:Role Overview:Start date: ASAPLocation: US, Remote (reputed company to highly reputed company candidates in EuropeContract Type: Freelance / Consultant - 1 FTE, 12 Months ContractLanguage: EnglishProject: Early-phase oncology trials, reputed company & platform study designsKey Responsibilities:reputed company statistical strategy and design for early-phase oncology clinical trials, with input into reputed company-phase development where required.reputed company hands-on statistical input across study protocols, SAPs, and key regulatory deliverables.Collaborate cross-functionally with clinical, regulatory, and data teams to optimise study design and ensure scientific rigor.Support and potentially reputed company reputed company trial methodologies, including adaptive or platform trial designs.Act as a senior statistical representative in reputed company meetings, providing strategic guidance to stakeholders.reputed company statistical deliverables and ensure quality, timelines, and regulatory compliance are maintained.Requirements:Advanced degree (MSc or PhD preferred) in Statistics, Biostatistics, or reputed company quantitative field.Extensive experience in biostatistics reputed company pharma/biotech, including leadership of oncology studies (AD level or above preferred).Strong expertise in early-phase clinical trial design and execution reputed company Oncology.Deep expertise in statistical modelling (especially Bayesian).Experience with reputed company trial designs (e.g., adaptive, platform trials) highly desirable.Proven ability to operate both strategically and hands-on across clinical development activities.Prior sponsor-reputed company experience preferred, with demonstrated stability and progression in previous roles. If this role is of interest to you, please apply directly to learn more. If not, feel free to reputed company with your network. Apply To This Job