Senior Statistician

QPS Bioserve; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

QPS Bioserve is seeking a statistics specialist to provide robust statistical support for clinical trial design, analysis, and reporting in Hyderabad. The role involves developing and reviewing SAPs, performing sample size calculations, and interpreting complex trial data with cross-functional teams.

Ideal candidates hold a Master’s or PhD in statistics/biostatistics, with strong knowledge of trial methodology and SAS proficiency.

Qualifications

• Master's or PhD in Statistics, Biostatistics, or a related field.
• Strong knowledge of clinical trial methodology and statistics.
• Proficiency in SAS and/or other tools.
• Experience across Phase III trials and sample size calculations.
• Strong communication and problem-solving skills.

Responsibilities

• Provide statistical support for clinical trial design, analysis, and reporting.
• Perform sample size and power calculations.
• Develop/review SAPs and statistical methods.
• Analyze and interpret clinical trial data and review tables, listings, and figures (TLFs).
• Experience with vasoconstriction, PD markers, immunogenicity, safety/efficacy endpoints is preferred.
• Collaborate with Clinical, Data Management, Programming, and Medical teams.
• Support CSRs and regulatory submissions.

Skills

Clinical trial statistics knowledge

Sample size calculations

Statistical analysis & interpretation

Communication & problem-solving

Cross-functional collaboration

Education

Master's/PhD in Statistics/Biostatistics or related field

Tools

SAS

Job description

Role & responsibilities:

• Statistical support for clinical trial design, analysis, and reporting.
• Sample size and power calculations.
• Develop/review Statistical Analysis Plans (SAPs) and statistical methods.
• Analyze and interpret clinical trial data and review TLFs.
• Experience with vasoconstriction, PD markers, immunogenicity, safety/efficacy endpoints, and other clinical biomarkers is preferred.
• Collaborate with Clinical, Data Management, Programming, and Medical teams.
• Support CSRs and regulatory submissions.

Requirements:

• Master's/PhD in Statistics, Biostatistics, or related field.
• Strong knowledge of clinical trial methodology and statistical methods.
• Proficiency in SAS and/or other tools.
• Experience across Phase IIII trials and sample size calculations.
• Strong communication and problem-solving skills.