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Biostatistician

Syngene
Syngene
2-5 years
Not Disclosed
10 Jan. 19, 2026
Job Description
Job Type: Full Time 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

Job Title: Biostatistician – Clinical Trials
Location: Semicon Park, Bangalore, India
Employment Type: Full-Time, Permanent
Department: Biostatistics and SAS Programming (BDM)
Experience Required: 2–5 years in clinical trial biostatistics


About Syngene

Syngene International Ltd. is a global contract research, development, and manufacturing organization (CRDMO) offering integrated scientific services from early discovery to commercial supply. With a strong focus on innovation, Syngene supports clients in pharmaceuticals, biotechnology, nutrition, and specialty chemicals, enabling faster drug development and data-driven decision-making for global clinical programs.


Role Summary

The Biostatistician will perform statistical and analytical functions to support clinical trials (Phase I–IV) within the Biometrics Department. The role involves statistical planning, data analysis, and reporting to ensure regulatory compliance, data integrity, and high-quality scientific outputs.


Key Responsibilities

  • Review study protocols and statistical analysis plans (SAPs).

  • Prepare and implement Randomization Allocation Plans (RAPs) and perform sample size calculations.

  • Provide statistical consultation to clinical teams.

  • Prepare and review randomization lists.

  • Perform statistical analyses according to SAP and protocol specifications.

  • Review SDTM and ADaM datasets for consistency and compliance.

  • Prepare and review tables, listings, and graphs (TLGs).

  • Draft and review statistical reports and documentation.

  • Support blinding and unblinding procedures as per protocol requirements.

  • Develop and review standard operating procedures (SOPs) for biostatistics processes.

  • Mentor and train associate biostatisticians and junior programmers.

  • Address statistical queries from clients and internal stakeholders.

  • Contribute to process improvement and ensure adherence to ICH-GCP and regulatory standards.


Educational Qualifications & Experience

  • M.Sc. or Ph.D. in Statistics or equivalent.

  • Strong expertise in SAS programming language.

  • Hands-on experience in clinical trials (Phase I–IV), including pharmacokinetics (PK) studies.

  • 2–5 years of professional experience in biostatistics within the pharmaceutical or clinical research industry is preferred.


Technical Skills

  • SAS programming and data management for clinical trials

  • Clinical trial design, sample size calculation, and statistical analysis

  • Knowledge of SDTM and ADaM data standards

  • TLG generation and statistical report writing

  • Strong understanding of GxP, ICH-GCP guidelines, and regulatory compliance

  • Data visualization and interpretation skills


Behavioral & Functional Skills

  • Analytical thinking and problem-solving

  • Team player with strong collaboration skills

  • Excellent communication, presentation, and scientific writing skills

  • Mentorship and knowledge transfer capabilities


Why Join Syngene?

  • Work on global clinical trials with cutting-edge statistical tools.

  • Collaborate with cross-functional clinical teams in a highly innovative environment.

  • Opportunity for professional growth and leadership in biostatistics.

  • Contribute to Syngene’s mission of delivering data-driven insights for faster drug development.


Equal Opportunity Employer

Syngene International Ltd. is committed to providing equal employment opportunities (EEO) to all candidates, regardless of age, gender, race, disability, religion, sexual orientation, or any legally protected characteristic. Reasonable accommodations are provided for qualified individuals with disabilities.