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Sr Biostatistician

0-2 years
Not Disclosed
10 Sept. 19, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Biostatistician

📍 Location: Pune, India – Hybrid
🆔 Job ID: 25101343
📅 Updated: September 17, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that combines clinical, medical affairs, and commercial expertise to accelerate customer success.

  • Global Workforce: 29,000 employees across 110 countries

  • Impact: Partnered on 94% of FDA-approved novel drugs (last 5 years) and 95% of EMA-authorized products

  • Clinical Reach: Supported over 200 studies across 73,000 sites and 675,000+ trial patients

💡 Work Here Matters Everywhere


Why Join Us?

  • Career growth & development opportunities

  • Supportive and engaged line management

  • Technical and therapeutic training

  • Peer recognition & rewards programs

  • Total Self Culture – be your authentic self

  • Inclusive, diverse, and collaborative workplace


Role Summary

The Senior Biostatistician will play a key role in supporting clinical development by applying statistical expertise to the design, analysis, and interpretation of clinical trials and studies.

You will collaborate across functions to ensure high-quality statistical deliverables that support regulatory submissions and scientific publications.


Key Responsibilities (typical for a Senior Biostatistician role)

(Note: The job description did not specify detailed duties. Below are the standard core responsibilities for this role in Syneos Health.)

  • Provide statistical input into study design, protocol development, and statistical analysis plans (SAPs)

  • Perform statistical analyses of clinical trial data using industry-standard software (e.g., SAS, R)

  • Ensure accuracy, consistency, and compliance of statistical deliverables with regulatory guidelines (FDA, EMA, ICH)

  • Collaborate with cross-functional teams including Clinical, Data Management, Programming, and Medical Writing

  • Contribute to clinical study reports, regulatory submissions, and publications

  • Support process improvement initiatives to enhance efficiency and quality of statistical deliverables

  • Mentor junior statisticians or biostatisticians when required


Qualifications & Skills

  • Advanced degree (Master’s or PhD) in Biostatistics, Statistics, or related field

  • Strong experience in statistical analysis of clinical trial data

  • Proficiency in SAS (mandatory) and/or R

  • Knowledge of regulatory requirements (FDA, EMA, ICH E9/E10)

  • Excellent problem-solving and analytical skills

  • Strong written and verbal communication abilities

  • Ability to work effectively in a cross-functional, global team environment


Other Information

  • Tasks and duties may be reassigned at the company’s discretion

  • Equivalent education/experience may be considered in place of listed qualifications

  • Syneos Health is committed to equal opportunity, diversity, and ADA compliance


👉 Apply Now or Join our Talent Network to stay connected with upcoming opportunities.

🔗 Learn more: www.syneoshealth.com