Statistical Programmer

Syneos Health

Lead statistical programmer developing SAS datasets, tables and graphs for Syneos Health’s clinical-trial services. Guiding programming teams, validating outputs and supporting sponsors throughout drug development.

Posted 8/11/2026full-timePune • 🇮🇳 IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive programming experience in SAS, with a strong focus on developing custom code for statistical analysis in clinical trial environments. Capable of managing project timelines, ensuring quality outputs, and mentoring programming personnel while adhering to regulatory guidelines.

Highest-signal resume keywords

SAS ProgrammingStatistical Analysis PlansClinical Trial ExperienceRegulatory Guidelines (ICH)Project Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Custom Programming Code DevelopmentValidation ProgrammingData Listings GenerationGraph CreationDerived Datasets CreationQuality ControlDataset Specifications DevelopmentProgramming Specifications ReviewStatistical Programming LeadershipDocumentation Maintenance

Soft Skills

Excellent Written CommunicationExcellent Verbal CommunicationTeam CollaborationMentoringProblem Solving

Industry Keywords

SOPsWork InstructionsRegulatory ComplianceClinical TrialsBiostatistics

About the role

Key responsibilities & impact

Develop custom programming code using SAS or other software to generate summary tables, data listings, graphs and derived datasets according to statistical analysis plans and programming specifications
Ensure outputs meet quality standards and project requirements
Perform validation programming and resolve discrepancies with Programmers, Biostatisticians and project team members
Keep project team members informed of programming progress and issues
Follow applicable SOPs, WIs and relevant regulatory guidelines such as ICH
Maintain complete, current project documentation, testing, verification and quality-control documents and programs
Manage schedules and time constraints across multiple projects and adapt workload to changing priorities
Develop specifications for datasets and outputs of any complexity
Anticipate and address programming issues to support efficient programming and peer or sponsor review
Prepare for and conduct effective internal meetings, distribute information and minutes, and track action items
Negotiate time estimates and complete study programming activities within allotted timeframes
Act as lead statistical programmer, direct other programming personnel and monitor deliverables
Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs and SAS database designs
Participate in sponsor, kickoff and bid defense meetings as the statistical programming representative
Mentor programming personnel through training, work review, feedback and process guidance
Transfer deliverables and perform other assigned work-related duties

Requirements

What you’ll need

Undergraduate degree, preferably in a scientific or statistical discipline
In lieu of a degree, an equivalent combination of education and demonstrated programming experience
Extensive programming experience in SAS or other required software, preferably in a clinical trial environment
Excellent written and verbal communication skills
Ability to read, write, speak and understand English
Knowledge of applicable SOPs, work instructions and relevant regulatory guidelines such as ICH

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
Inclusive culture
Comprehensive resources including emerging technologies, data, science and knowledge sharing
Minimal travel may be required