Location: India (Remote)
Company: Syneos Health
Job ID: 25107198
Experience Required: 4–8 years (Not suitable for freshers)
About the Company
Syneos Health is a leading global contract research and biopharmaceutical solutions organization that supports clinical development, data science, and commercialization across the healthcare ecosystem. With a strong global presence and expertise across therapeutic areas, the company is known for accelerating drug development and improving patient outcomes.
Job Overview
The Sr. Statistical Programmer is responsible for delivering high-quality statistical programming outputs to support clinical trials and regulatory submissions. This role involves working closely with Biostatisticians, Clinical Data teams, and sponsors to develop analysis datasets, tables, listings, and figures in compliance with global regulatory standards.
Key Responsibilities
Develop and validate SAS programming code to generate Tables, Listings, and Figures (TLFs) as per Statistical Analysis Plan (SAP)
Create and maintain derived datasets in compliance with CDISC standards (SDTM/ADaM)
Perform quality control (QC) and validation programming to ensure accuracy and consistency of outputs
Collaborate with Biostatisticians and cross-functional teams to resolve data discrepancies and programming issues
Review key study documents including SAPs, annotated CRFs, mock shells, and programming specifications
Lead statistical programming activities for assigned studies and oversee deliverables of junior programmers
Ensure timely completion of programming milestones while maintaining high-quality standards
Participate in sponsor meetings, kickoff discussions, and bid defense activities as required
Maintain audit-ready documentation, including validation reports and QC logs
Ensure compliance with ICH guidelines, SOPs, and global regulatory requirements
Required Qualifications
Bachelor’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field
4–8 years of hands-on experience in SAS programming within a clinical trial environment
Strong expertise in CDISC standards (SDTM and ADaM) and regulatory submission requirements
Proficiency in SAS/Base, SAS/Macro, and data manipulation techniques
Excellent problem-solving, analytical, and communication skills
Ability to manage multiple projects and work in a remote, global team environment
Preferred Skills
Experience in leading programming activities for clinical trials
Exposure to regulatory submissions (FDA/EMA)
Knowledge of advanced statistical methods and data visualization tools
Why This Role Matters
Work on global clinical trials contributing to drug development and regulatory approvals
Opportunity to lead programming deliverables in a remote-first global setup
High visibility role with cross-functional and sponsor interaction
Strong career growth in biostatistics and statistical programming domain
Important Note for Applicants
This is a senior-level role requiring prior clinical SAS programming experience. Freshers are advised to begin with entry-level roles such as Statistical Programming Trainee, Clinical Data Analyst, or SAS Programmer (Junior) before progressing to senior positions like this.
How to Apply
Apply through the official careers page or trusted job platforms. For verified global clinical research and pharmacovigilance opportunities, explore ThePharmaDaily.com
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