This is a pre-market vacancy. The search will begin by the end of November '25. Apply now to be considered ahead of the rest of the market.

Role Summary

A clinical-stage oncology biotech is looking to engage an experienced Associate Director of Biostatistics to lead statistical efforts for key clinical development programs – reporting to the Head of Biometrics.



Responsibilities:

• Serve as the lead Biostatistician for ongoing and planned oncology trials, including late-phase studies.
• Author and review statistical documents including protocol sections, SAPs, and TLF shells.
• Collaborate cross-functionally with Clinical Development, Data Management, and Regulatory to guide study design and analysis strategies.
• Oversee CRO partners to ensure statistical deliverables are timely, accurate, and compliant.
• Contribute to data interpretation, reporting, and health authority interactions.
• Provide strategic input to biometrics planning across a growing clinical pipeline.

Requirements:

• Advanced degree (PhD or Master’s) in Biostatistics or a related field.
• Strong experience in Biostatistics within the biotech or pharma industry, ideally in oncology.
• Demonstrated ability to lead studies independently and interact cross-functionally.
• Familiarity with regulatory standards and submission-readiness practices.
• Excellent communication and stakeholder management skills.

Salary based on experience and will be provided after search kickoff