Senior Statistician (Biostatistician)

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

Job summary

QPS Bioserve invites a qualified statistician to provide statistical support for clinical trial design, analysis, and reporting.

You will perform sample size and power calculations, develop or review SAPs and statistical methods, and analyze trial data, including interpretation of endpoints and biomarkers.

Collaborating with Clinical, Data Management, Programming, and Medical teams, you will support CSRs and regulatory submissions while communicating findings clearly.

Qualifications

• Master's or PhD in Statistics, Biostatistics, or related field.
• Strong knowledge of clinical trial methodology and statistics.
• Experience with sample size calculations.
• Excellent communication and problem-solving skills.

Responsibilities

• Provide statistical support for trial design, analysis, and reporting.
• Perform sample size and power calculations.
• Develop/review SAPs and statistical methods.
• Analyze and interpret trial data and review TLFs.
• Collaborate with Clinical, Data Management, Programming, and Medical teams.
• Support CSRs and regulatory submissions.

Skills

Statistical methods

Clinical trial methodology

Communication

Problem-solving

Education

Master's degree in Statistics/Biostatistics

PhD in Statistics/Biostatistics (preferred)

Tools

SAS

Other tools

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.