Senior Biostatistician for inhouse project (Permanent role)

ClinChoice

6h • Remote

About The Position

ClinChoice is seeking a highly skilled Senior Statistician for a permanent, in-house position to lead and support statistical activities for clinical trials. This role offers the opportunity to work directly for a single sponsor while benefiting from the security and career opportunities of a global CRO. The ideal candidate will possess hands-on statistical expertise, strong communication skills, and the ability to independently lead projects while collaborating with cross-functional teams in a dynamic environment.

Requirements

• MS or PhD in Statistics, Biostatistics, or a related field
• Strong experience in Immunology or any TA clinical studies
• Hands-on experience writing: Statistical Analysis Plans (SAPs)
• Hands-on experience writing: Analysis Database Specifications
• Reviewing and interpreting analysis results
• SAS programming skills required (hands-on or strong working knowledge)
• Excellent written and verbal communication skills
• Experience working in a CRO and/or pharmaceutical/biotech environment

Nice To Haves

• Experience leading Phase II–III clinical trials
• Prior interaction with regulatory agencies
• Experience mentoring junior statisticians or programmers

Responsibilities

• Lead and provide statistical support for clinical studies, primarily within Immunology or any therapeutic areas
• Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables
• Author and review key statistical documents, including: Statistical Analysis Plans (SAPs), Analysis Database Specifications (ADS), Statistical sections of clinical study reports
• Review and interpret analysis outputs, ensuring accuracy, quality, and regulatory compliance
• Collaborate with cross-functional teams including Clinical, Programming, Data Management, and Regulatory
• Provide guidance and oversight to statistical programmers as needed
• Communicate statistical concepts, results, and risks clearly to both technical and non-technical stakeholders
• Ensure adherence to regulatory standards (FDA, ICH, GCP) and company SOPs

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree