Principal Biostatistician for inhouse project (Permanent role)

United StatesOn-site

Responsibilities

Lead and provide statistical support for clinical studies, primarily within Immunology or any therapeutic areas •
Author and review key statistical documents, including: •
Review and interpret analysis outputs, ensuring accuracy, quality, and regulatory compliance •
Collaborate with cross-functional teams including Clinical, Programming, Data Management, and Regulatory •
Ensure adherence to regulatory standards (FDA, ICH, GCP) and company SOPs Required

This role requires hands-on statistical expertise, strong communication skills, and the ability to independently lead projects while collaborating closely with cross-functional teams. Key Responsibilities •
MS or PhD in Statistics, Biostatistics, or a related field • Strong
experience in Immunology or any TA clinical studies •
SAS programming skills required (hands-on or strong working knowledge) •
Experience working in a CRO and/or pharmaceutical/biotech environment Preferred
Experience leading Phase II–III clinical trials •
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...
ClinChoice is currently recruiting for a Principal Statistician to join our team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment. Job Summary
We are seeking a highly skilled Principal Statistician to lead statistical activities for clinical trials.
Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables •
Provide guidance and oversight to statistical programmers as needed •
Communicate statistical concepts, results, and risks clearly to both technical and non-technical stakeholders •