Senior Statistical Programmer

Syneos Health

. Use SAS or other software to develop custom programming code for summary tables, data listings, graphs, and derived datasets .

Posted 9/18/2026full-timeRemote • IndiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive programming experience in SAS for clinical trial outputs, with a strong ability to lead statistical programming activities and mentor programming personnel. Proficient in managing multiple projects while ensuring compliance with regulatory guidelines and quality standards.

Highest-signal resume keywords

SAS ProgrammingStatistical Analysis PlansClinical Trial OutputsProject ManagementMentoring Programming Personnel

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Custom Programming Code DevelopmentValidation ProgrammingData ListingsSummary TablesGraphsDerived DatasetsSAS Database DesignStatistical ProgrammingQuality ControlDocumentation Maintenance

Soft Skills

Excellent Written CommunicationExcellent Verbal CommunicationTeam CollaborationFeedback ProvisionAction Item Follow-Up

Industry Keywords

Clinical Trial EnvironmentICH GuidelinesSOPsWork InstructionsRegulatory Guidelines

About the role

Key responsibilities & impact

Use SAS or other software to develop custom programming code for summary tables, data listings, graphs, and derived datasets
Ensure outputs meet quality standards and project requirements
Perform validation programming and resolve discrepancies with Programmers, Biostatisticians, and project team members
Maintain complete, current project documentation, testing, and quality control materials for inspection readiness
Manage scheduling and time constraints across multiple projects
Develop specifications for datasets and outputs according to statistical and sponsor requirements
Prepare for and conduct internal meetings, distribute information and minutes, and follow action items through completion
Estimate and complete study programming activities within allotted timelines
Act as lead statistical programmer and direct programming activities of other personnel
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 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 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
Ability to develop custom programming code for clinical trial outputs
Knowledge of statistical analysis plans, programming specifications, annotated CRFs, and SAS database design
Knowledge of applicable SOPs, work instructions, and relevant regulatory guidelines such as ICH
Ability to lead statistical programming activities and direct other programming personnel
Ability to manage multiple projects, schedules, priorities, and timelines
Ability to participate in sponsor, kickoff, and bid defense meetings
Ability to mentor programming personnel and provide feedback

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition
Total rewards program
Inclusive culture
Minimal travel may be required