About Sigma-Chi Consulting
With more than a decade of experience, Sigma-Chi Consulting is a trusted biometrics partner to pharmaceutical and biotech sponsors, with teams in Hyderabad and Visakhapatnam supporting clients in the USA and Europe. We deliver biostatistics, statistical programming, clinical data management and AI-driven TLF quality control, with a strong focus on quality and on-time delivery.
Job Overview
As a Biostatistician II you will provide statistical input from study design through analysis and reporting for Phase I–IV clinical trials.
Key Responsibilities
- Contribute to protocol statistical sections, sample size and power calculations
- Write Statistical Analysis Plans (SAPs) and TLF mock shells
- Generate randomization schedules
- Review programmed outputs for accuracy and consistency
- Interpret results and support Clinical Study Report (CSR) writing
- Interact with sponsors and cross-functional teams on statistical matters
Requirements
- Master’s or PhD in Statistics or Biostatistics
- 4–8 years of experience as a biostatistician in pharma or a CRO
- Strong knowledge of statistical methods for clinical trials, including mixed models, survival analysis and categorical data analysis
- Proficiency in SAS and/or R
- Knowledge of ICH E9 (R1) and estimands
Good to have
- Experience with adaptive or Bayesian designs
- Regulatory submission experience (FDA, EMA, PMDA)
What we offer
- Work on global pharma and biotech studies across therapeutic areas
- Mentoring from senior programmers and statisticians
- Exposure to our in-house AI tools for clinical reporting
- A collaborative team with clear career growth paths
How to apply
Use the Quick Apply button on this page, or send your CV to hr@sigma-chiconsulting.com with the job title in the subject line.
Job Features
| Job Category | Biostatistics |