An East-Coast clinical-stage Biopharma seeks an experienced Contract Biostatistician.

Responsibilities:

• Lead day-to-day statistical activities across Phase II and III studies.
• Conduct hands-on analyses and contribute to ad hoc requests.
• Draft and review key statistical documentation, including contributing to protocol sections, SAPs, and CSRs.
• Oversee statistical deliverables from CROs and vendors - ensuring high-quality, timely outputs.
• Work closely with stakeholders across Clinical Operations, Development, Regulatory, and other functional areas.

Requirements:

• Advanced degree (PhD or Master’s) in Biostatistics or closely related field.
• Significant experience in Biostatistics within the life sciences sector.
• Proven track record supporting Phase II/III studies.
• Comfortable overseeing CRO/vendor work and holding partners to a high standard.
• Excellent communication skills with the ability to simplify complex statistical ideas for non-technical colleagues.

Rate dependent on experience and engagement type