EPM Scientific 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 complex oncology studies, including early-phase trial design. See a summary of the role below: Role Overview:

• Start date: ASAP
• Location: US, Remote (Open to highly qualified candidates in Europe
• Contract Type: Freelance / Consultant - 1 FTE, 12 Months Contract
• Language: English
• Project: Early-phase oncology trials, complex & platform study designs

Key Responsibilities:

• Lead statistical strategy and design for early-phase oncology clinical trials, with input into later-phase development where required.
• Provide 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 lead complex trial methodologies, including adaptive or platform trial designs.
• Act as a senior statistical representative in internal and external meetings, providing strategic guidance to stakeholders.
• Oversee statistical deliverables and ensure quality, timelines, and regulatory compliance are maintained.

Requirements:

• Advanced degree (MSc or PhD preferred) in Statistics, Biostatistics, or related quantitative field.
• Extensive experience in biostatistics within pharma/biotech, including leadership of oncology studies (AD level or above preferred).
• Strong expertise in early-phase clinical trial design and execution within Oncology.
• Deep expertise in statistical modelling (especially Bayesian).
• Experience with complex trial designs (e.g., adaptive, platform trials) highly desirable.
• Proven ability to operate both strategically and hands-on across clinical development activities.
• Prior sponsor-side 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 share with your network.