Contract Biostatistician (hybrid)
CA, USA
Apply for this job

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




Apply for this job
Powered by