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Sr Biostatistician

Syneos Health
4+ years
INR 12 LPA – 15 LPA
Remote, India, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

 

Sr. Biostatistician

Company: Syneos Health
Location: Remote (India)
Job ID: 25109187
Employment Type: Full-Time
Work Mode: Remote

About the Role

Syneos Health is hiring a Sr. Biostatistician to support clinical research and drug development programs. The role involves statistical analysis, study design support, interpretation of clinical trial data, and collaboration with cross-functional teams to ensure high-quality statistical deliverables across clinical studies.

Key Responsibilities

  • Perform statistical analyses for clinical trials and research studies.

  • Develop and review Statistical Analysis Plans (SAPs).

  • Support clinical study design, sample size calculations, and protocol development.

  • Generate statistical outputs including tables, listings, and figures (TLFs).

  • Interpret and present statistical findings to project teams and stakeholders.

  • Collaborate with Clinical Data Management, Programming, Medical Writing, and Clinical Operations teams.

  • Ensure compliance with regulatory requirements and industry standards.

  • Support regulatory submissions and responses to health authorities.

  • Participate in study planning, execution, and reporting activities.

  • Maintain high-quality statistical documentation and deliverables.

Required Qualifications

Education:

  • M.Sc. (Statistics/Biostatistics)

  • PhD (Statistics/Biostatistics)

  • Mathematics

  • Life Sciences with Biostatistics Specialization

  • Equivalent Quantitative Degree

Experience:

  • Typically 4+ years of Biostatistics experience within CRO, Pharmaceutical, Biotechnology, or Clinical Research organizations.

  • Experience supporting clinical trials and statistical analysis activities.

  • Knowledge of regulatory requirements and clinical research processes preferred.

Required Skills

  • Biostatistics

  • Statistical Analysis

  • Clinical Trials

  • Statistical Analysis Plans (SAP)

  • SAS Programming

  • Data Interpretation

  • Clinical Research

  • TLF Generation

  • Regulatory Submissions

  • Clinical Data Analysis

  • ICH Guidelines

  • Drug Development Process

Preferred Candidate Profile

  • Experience working in CRO or Pharmaceutical industry.

  • Strong analytical and problem-solving skills.

  • Expertise in SAS and statistical methodologies.

  • Ability to work independently in a remote environment.

  • Excellent communication and stakeholder management skills.