A California-based, clinical-stage biotech company is seeking an experienced Contract Biostatistician at the Principal or Associate Director level. This role has the potential to transition to a permanent position around the end of 2025.

Key Responsibilities:

• Provide study-level oversight and manage daily operations for Phase II and Phase III trials.
• Engage in hands-on statistical analysis.
• Provide ad hoc analysis as required
• Write the statistical section of the protocol, author SAP, review CSR, and other trial related documentation
• Oversee and collaborate with relationships with external vendors and quality check inbound deliverables
• Operate cross-functionally, alongside other key business units: Clinical Operations, Clinical Development, Regulatory Affairs, etc.

Qualifications:

• PhD or Master's with supplementary experience in Biostatistics or related field.
• Proven experience working for a Pharma / Biotech.
• Strong Phase II and III experience.
• Well versed working with external CRO/Vendor partners
• Strong communication skills, both written and oral, and a keen ability to communication statistical concepts to non-statistically minded individuals.

Rate dependent on experience and engagement type - $100 - $150 per hour