EPM Scientific is supporting an innovative biotechnology company that is expanding its Biostatistics capabilities. This role offers the opportunity to contribute to an. Project Overview: Project Type: Solid Tumours, Oncology Location: Anywhere in United States, Fully Remote Contract Type: Contract, 9 Months Start Date: As soon as possible Language Requirements: Englsih Key Responsibilities: Lead statistical aspects of clinical trials, ensuring high‑quality analyses, documentation, and regulatory‑ready deliverables. Partner cross‑functionally with Clinical, Regulatory, Programming, Data Management, and Safety teams to support development strategy. Contribute to regulatory submissions and interactions, including statistical sections of INDs, NDAs/BLAs, and briefing materials. Oversee and mentor statisticians, ensuring strong technical execution and resource alignment across projects. Drive use of modern statistical methods and best practices to enhance scientific and operational quality. Support publications, presentations, and external communication of study results. Requirements: Strong experience (8 years preferred) in Biostatistics strongly preferred. Experience with Submissions is essential. Experience with Solid Tumors is strongly preferred. Advanced degree in life sciences, medicine, or pharmacy preferred. Ability to work independently, with excellent communication and stakeholder engagement skills. If this position sounds interesting, please apply directly.