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Sr Biostatistician

Syneos Health
Syneos Health
5-8 years
upto 12 LPA
Remote, India, India
8 April 23, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Master’s or PhD in Biostatistics, Statistics, or related quantitative field 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 – RWE & Clinical Trials

Location: India (Remote)
Company: Syneos Health
Job ID: 25107212
Experience Required: 5–8 years (Not suitable for freshers)


About the Company

Syneos Health is a leading global biopharmaceutical solutions organization that accelerates drug development and commercialization. With a strong presence across clinical research, real-world evidence (RWE), and data-driven healthcare solutions, the company collaborates with innovators to bring life-changing therapies to market faster.


Job Overview

The Senior Biostatistician will play a key role in designing, analyzing, and interpreting clinical trial and real-world data. This position focuses on statistical leadership across study phases, ensuring scientific rigor, regulatory compliance, and high-quality deliverables in clinical development programs.


Key Responsibilities

  • Lead statistical activities for clinical trials and real-world evidence (RWE) studies

  • Develop and review Statistical Analysis Plans (SAPs), mock shells, and study outputs

  • Perform advanced statistical analysis using R and SAS for efficacy and safety data

  • Contribute to Clinical Study Reports (CSR) and regulatory submissions

  • Support randomization processes and statistical design methodologies

  • Apply estimand framework principles in clinical trial analysis

  • Utilize Bayesian statistical methods where applicable

  • Work with diverse datasets including Electronic Health Records (EHR), claims data, and patient registries

  • Ensure compliance with CDISC standards and global regulatory guidelines

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


Required Qualifications

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

  • 5–8 years of experience in biostatistics within clinical research or CRO environment

  • Strong proficiency in R (mandatory) and SAS

  • Hands-on experience with RWE data sources such as EHR, claims, or registries

  • Experience in SAP development, CSR review, and statistical modeling

  • Knowledge of CDISC standards and clinical trial phases

  • Exposure to Oncology or other therapeutic areas is an advantage

  • Strong analytical thinking and communication skills


Preferred Skills

  • Experience in Bayesian statistics and advanced modeling techniques

  • Prior experience as Lead Biostatistician in global clinical trials

  • Understanding of estimand framework and regulatory expectations


Why This Role Stands Out

  • Work remotely on global clinical and RWE projects

  • Opportunity to contribute to high-impact drug development programs

  • Exposure to cutting-edge statistical methodologies and large-scale healthcare datasets

  • Collaborative environment with global experts in clinical research and data science


Important Note for Applicants

This is a senior-level role requiring hands-on experience in biostatistics and clinical trials. Freshers or entry-level candidates should consider roles such as Statistical Programmer, Junior Biostatistician, or Clinical Data Analyst to build foundational experience before applying for senior positions.


How to Apply

Apply directly through the official careers page or trusted job platforms. For more verified global opportunities in Biostatistics, Clinical Research, and Pharmacovigilance, explore ThePharmaDaily.com