ClinChoice
SeniorBiostatistician
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“Senior Biostatistician at ClinChoice. Skills: Biostatistics, Statistical Analysis, Clinical Trials, SAS, R. Provide statistical support for Phase I–IV clinical trials. Participate in protocol development, study design, and sample size calculations”
Industry & Context.
excellent problem-solving skills
What They're Looking For.
Must Have
Master's or PhD in Statistics, Biostatistics, Mathematics, or related field, Minimum 5–8 years of experience in biostatistics within CRO, pharmaceutical, or biotech industry, knowledge of clinical trial methodology and statistical principles, Experience with SAS and/or R programming, Familiarity with CDISC standards (SDTM/ADaM), Excellent communication, problem-solving, and organizational skills, Ability to manage multiple projects and work independently
Nice to Have
Experience supporting regulatory submissions
What You'll Do.
Provide statistical support for Phase I–IV clinical trials
Participate in protocol development
and sample size calculations
Prepare and review Statistical Analysis Plans (SAPs)
and randomization specifications
Perform statistical analyses and interpret study results
and figures for accuracy and consistency
Support regulatory submissions including ISS/ISE and responses to health authority queries
Ensure compliance with CDISC
and regulatory guidelines
Contribute to process improvements and mentoring of junior statisticians
Participate in client meetings and provide statistical expertise to sponsors
How You'll Work.
Team & Collaboration
Collaborate with Clinical Data Management, Statistical Programming, Medical Writing, and Clinical Operations teams; Collaborate with cross-functional teams
Communication Scope
excellent communication skills; provide statistical expertise to sponsors; participate in client meetings
Process & Methodology
Ability to manage multiple projects
Full Job Description
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 Senior 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 an experienced and highly motivated Senior Statistician to join our Biometrics team. The successful candidate will provide statistical support for clinical trials across multiple therapeutic areas and contribute to study design, protocol development, statistical analysis, and regulatory submissions. This role requires strong technical expertise, excellent communication skills, and the ability to collaborate with cross-functional teams in a fast-paced CRO environment. Key Responsibilities Provide statistical support for Phase I–IV clinical trials. Participate in protocol development, study design, and sample size calculations. Prepare and review Statistical Analysis Plans (SAPs), TLF shells, and randomization specifications. Perform statistical analyses and interpret study results. Collaborate with Clinical Data Management, Statistical Programming, Medical Writing, and Clinical Operations teams. Review outputs, tables, listings, and figures for accuracy and consistency. Support regulatory submissions including ISS/ISE and responses to health authority queries. Ensure compliance with CDISC, ICH-GCP, and regulatory guidelines. Contribute to process improvements and mentoring of junior statisticians. Participate in client meetings and provide statistical expertise to sponsors. Required Qualifications Master’s or PhD in Statistics, Biostatistics, Mathematics, or related field. Minimum 5–8 years of experience in biostatistics within CRO, pharmaceutical, or biotech industry. Strong knowledge of clinical trial methodology and statistical principles. Exper
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