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.

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.
Experience with SAS and/or R programming.
Familiarity with CDISC standards (SDTM/ADaM).
Experience supporting regulatory submissions is preferred.
Excellent communication, problem-solving, and organizational skills.
Ability to manage multiple projects and work independently

Senior Biostatistician – Permanent role

Key skills