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Posted 1 weeks agoPrincipal Biostatistician for inhouse project (Permanent role)
at ClinChoice
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
Requirements
- 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
Additional details
- 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 •