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Sr Biostatistician

Syneos Health
5-10 years
INR 18 LPA – 35 LPA
Remote, India, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Sr Biostatistician

Company: Syneos Health
Location: India (Remote)
Work Mode: Remote
Employment Type: Full-Time

Job Overview

The Sr Biostatistician is responsible for leading statistical design, analysis, and interpretation of clinical trial data across multiple studies. The role involves collaboration with cross-functional clinical, data management, and regulatory teams to ensure high-quality statistical deliverables that support clinical development and regulatory submissions. The position requires strong expertise in biostatistics methodologies and the ability to operate in a fast-paced global CRO environment.

Key Responsibilities

  • Lead statistical design, methodology, and analysis planning for clinical trials

  • Develop and review Statistical Analysis Plans (SAPs) and related documentation

  • Perform statistical programming oversight and ensure accuracy of study outputs

  • Collaborate with clinical teams, data managers, and programmers on study deliverables

  • Provide input on study design, sample size determination, and endpoint selection

  • Review TLFs (Tables, Listings, Figures) and ensure statistical validity

  • Support regulatory submissions and respond to health authority queries

  • Ensure compliance with CDISC standards and regulatory guidelines

  • Provide statistical expertise during audits and inspections

  • Contribute to study protocols, CSR review, and integrated summaries

  • Mentor junior statisticians and provide technical guidance

  • Participate in cross-functional project meetings and sponsor discussions

  • Ensure timely delivery of statistical deliverables across multiple studies

Required Qualifications

  • Master’s or PhD in Statistics, Biostatistics, Mathematics, or related quantitative field

  • Strong knowledge of clinical trial methodology and statistical principles

  • Proficiency in statistical software (SAS required; R preferred)

  • Understanding of CDISC standards (SDTM, ADaM)

  • Knowledge of ICH-GCP and regulatory requirements

Preferred Qualifications

  • Experience working in CRO or pharmaceutical industry

  • Exposure to global clinical trial submissions (FDA/EMA)

  • Experience in oncology, rare diseases, or complex therapeutic areas

  • Experience in statistical consulting or leadership roles

  • Familiarity with real-world evidence or adaptive trial designs

Experience Required

  • 5–10+ years of experience in Biostatistics / Clinical Statistics

  • Experience in clinical trial design, analysis, and regulatory submission support