Principal Clinical Programmer (DM SAS) – Structured Job Format
Job Overview
Position: Principal Clinical Programmer (DM SAS)
Company: Syneos Health
Location: Hyderabad (Hybrid)
Job ID: 25106545
Updated: May 18, 2026
Department: Clinical Programming / Data Management
Work Mode: Hybrid
About the Company
Syneos Health is a global life sciences services organization focused on accelerating customer success across clinical development and commercialization.
Company highlights:
Supported 94% of novel FDA-approved drugs in the last 5 years
Worked on 95% of EMA-authorized products
Conducted 200+ studies across 73,000+ clinical sites globally
Role Summary
The Principal Clinical Programmer (DM SAS) serves as a senior technical lead responsible for:
Managing clinical programming activities across multiple studies
Supporting Data Management and EDC systems
Designing, developing, validating, and maintaining clinical programming solutions
Leading study build and SAS programming activities
Supporting integrations, reporting, and data processing systems
Mentoring junior programmers and coordinating project deliverables
This role requires strong expertise in Clinical Data Management (CDM), SAS programming, EDC systems, and leadership in clinical programming operations.
Key Responsibilities
Clinical Programming Leadership
Serve as Lead Clinical Programmer for:
Single studies
Multi-study programs
Manage project deliverables and timelines
Guide and mentor junior programmers
Coordinate clinical programming development activities
SAS Programming & Development
Design, write, validate, and maintain software applications
Develop:
SAS listings
SAS macros
Data import/export programs
Custom reports
Support:
Data acquisition
SAS mapping
Study builds
EDC & Clinical Systems Support
Work with clinical systems including:
Medidata Rave
Oracle OC/RDC
Oracle Inform
SAS platforms
Support:
Database creation
Edit checks
Coding configurations
Import/export setup and processing
Documentation & Validation
Generate and maintain:
Programming specifications
Validation documentation
Annotated CRFs
Study documentation
Ensure compliance with standard development procedures
Project Coordination
Participate in project meetings and development discussions
Communicate project risks, scope changes, and timeline concerns
Manage multiple concurrent studies (3–10 studies depending on scope)
Coordinate with:
Data Managers
Project Analysts
Clinical teams
Sponsors
Technical Support & Administration
Provide subject matter expertise for:
EDC systems
Reporting tools
Clinical programming applications
Monitor systems for:
Workflow alerts
System errors
Performance issues
Provide second-level technical support
Quality Assurance & Compliance
Perform senior-level review of:
Study deliverables
Program outputs
Clinical programming deliverables
Support sponsor audits and inspection readiness activities
Integration & Testing
Perform:
System integration activities
Application updates
User Acceptance Testing (UAT)
Team Leadership & Mentoring
Train and guide junior programmers
Support departmental skill development
Assist in resource planning and workload management
Budget & Scope Management
Review study budgets
Monitor scope versus actual work
Identify and manage change orders
Escalate resourcing concerns proactively
Required Qualifications
Educational Background
Bachelor’s degree preferred
OR
Equivalent combination of education and relevant experience
Experience Requirements
Minimum 6+ years of experience in:
DM SAS Clinical Programming
Clinical Data Management environments
Preferred Experience
Oversight of 4–5 studies simultaneously
SAS listings and macro development
Data imports and acquisition
Study build activities
SAS mapping
Lead programming experience
Technical Skills
Required Tools & Platforms
SAS
Medidata Rave
Oracle Inform
Oracle RDC / OC-RDC
Preferred Technical Skills
PL/SQL
C#
VB (Visual Basic)
Certifications
Preferred:
Base SAS Certification
Advanced SAS Certification
Required Competencies
Clinical & Technical Expertise
Clinical programming methodologies
Clinical data management workflows
EDC systems administration
Validation and QC processes
Study build and reporting systems
Project & Leadership Skills
Multi-project management
Resource coordination
Team leadership
Stakeholder communication
Soft Skills
Excellent verbal and written communication
Strong interpersonal and sponsor-facing skills
Analytical and problem-solving mindset
Ability to work in matrix-structured environments
Strong organizational and prioritization skills
Travel Requirement
Ability to travel up to 25% as required
Work Environment & Culture
Why Join Syneos Health?
Career development and growth opportunities
Technical and therapeutic-area training
Collaborative and inclusive culture
Exposure to global clinical development programs
Recognition and rewards programs
Functional Areas Covered
Clinical Programming
Data Management
SAS Programming
EDC Systems
Clinical Reporting
Database Build & Validation
Study Data Processing
Seniority & Impact
Role Level
Senior principal-level technical leadership role with:
Cross-study oversight
Team mentoring responsibilities
Sponsor interaction and operational ownership
Business Impact
This role contributes directly to:
Clinical data quality
Efficient study execution
Regulatory readiness
Delivery of clinical programming solutions
Ideal Candidate Profile
The ideal candidate should:
Have strong expertise in DM SAS programming
Lead multiple clinical studies independently
Understand EDC systems deeply
Manage sponsor and stakeholder interactions confidently
Mentor and support junior programmers
Deliver high-quality programming outputs within timelines
Employment Notes
Additional responsibilities may be assigned as needed
Equivalent qualifications and experience may be considered
Syneos Health is an equal opportunity employer
Reasonable accommodations are available where appropriate
Application
Apply via:
Syneos Health Careers
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