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Principal Stat Programmer

0-2 years
Not Disclosed
10 April 7, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Principal Statistical Programmer


Updated Date: March 28, 2025

Location: India-Asia Pacific - IND-Home-Based

Job ID: 25002564

Company: Syneos Health®


About the Company:

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, operating in 110 countries with 29,000 employees. Focused on accelerating customer success, Syneos brings clinical, medical affairs, and commercial insights to address modern market realities.


Why Join Syneos Health:

  • Career development and progression

  • Supportive management and training

  • Peer recognition and rewards programs

  • Inclusive “Total Self” culture

  • A global workplace that values diversity and belonging


Job Responsibilities:

  • Develops SAS or other programming code for tables, listings, graphs, and datasets as per analysis plans

  • Performs validation programming and resolves issues collaboratively

  • Maintains complete and inspection-ready documentation

  • Manages timelines across multiple projects

  • Leads programming teams and monitors deliverables

  • Reviews statistical documentation and provides feedback

  • Participates in client and internal meetings

  • Mentors junior programmers

  • Provides technical expertise in CDISC standards and regulatory submissions

  • Contributes to SOPs and programming tool development

  • Conducts compliance reviews for CDISC and regulatory standards

  • Performs other job-related duties as assigned

  • Minimal travel required


Qualifications:

  • Undergraduate degree in a scientific or statistical discipline (or equivalent experience)

  • Extensive SAS programming experience in a clinical trial setting

  • Knowledge of CDISC standards and experience with regulatory submissions

  • Experience mentoring others in clinical trial processes

  • Strong written and verbal English communication skills


Additional Notes:

  • The role may evolve; additional responsibilities may be assigned without prior notice

  • Equivalent experience/education may be considered

  • Reasonable accommodations provided per the Americans with Disabilities Act