Location: India (Remote)
Company: Syneos Health
Job ID: 25107306
Experience Required: 4–8 years (Not suitable for freshers)
About the Company
Syneos Health is a globally recognized biopharmaceutical solutions organization that accelerates drug development and commercialization. With a strong presence across clinical research and data sciences, the company partners with global sponsors to deliver high-quality, data-driven healthcare outcomes.
Job Overview
The Senior Statistical Programmer is responsible for developing, validating, and delivering statistical programming outputs for clinical trials. This role requires strong expertise in SAS programming, clinical data structures, and regulatory compliance, ensuring accurate and timely generation of analysis datasets, tables, listings, and figures.
Key Responsibilities
Develop and validate SAS programs to generate statistical outputs including tables, listings, and graphs (TLFs) as per Statistical Analysis Plans (SAP)
Create and manage derived datasets aligned with CDISC standards and sponsor requirements
Perform quality control and validation programming to ensure accuracy and regulatory compliance
Collaborate with Biostatisticians, Data Management, and Clinical teams to resolve discrepancies and optimize outputs
Review key study documents such as SAPs, annotated CRFs, mock shells, and programming specifications
Lead statistical programming activities and oversee deliverables across multiple clinical projects
Ensure inspection readiness by maintaining complete documentation, validation logs, and audit trails
Participate in sponsor meetings, study kick-offs, and bid defense presentations
Mentor junior programmers and contribute to training and capability development
Manage timelines, prioritize workloads, and proactively address risks in programming deliverables
Required Qualifications
Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, Life Sciences, or related field
4–8 years of statistical programming experience in a clinical trial or CRO environment
Strong proficiency in SAS programming (Base SAS, SAS/STAT, SAS Macro)
Experience with CDISC standards (SDTM, ADaM) and regulatory submission requirements
Solid understanding of ICH-GCP guidelines and clinical data workflows
Excellent communication, problem-solving, and stakeholder management skills
Preferred Skills
Experience leading programming teams or managing study-level deliverables
Exposure to regulatory submissions (FDA, EMA)
Ability to handle multiple global clinical projects in a remote environment
Why This Role Stands Out
Fully remote global opportunity with exposure to international clinical trials
Work on high-impact drug development programs across therapeutic areas
Opportunity to lead programming strategy and mentor teams
Strong career growth within a top-tier CRO ecosystem
Important Note for Applicants
This is a senior-level role requiring hands-on experience in statistical programming within clinical trials. Freshers are advised to start with entry-level roles such as Statistical Programmer I, SAS Programmer, or Clinical Data Analyst before applying to senior positions.
How to Apply
Apply through the official careers page of Syneos Health or explore verified global opportunities on ThePharmaDaily.com.
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