Associate Director Biostatistics

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.