Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

R Statistical Programmer – Submission Experience Required

Syneos Health
6+ years
INR 18 LPA – 28 LPA
Remote, India, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

R Statistical Programmer – Submission Experience Required

Company: Syneos Health
Location: Remote (India)
Job ID: 25108545
Employment Type: Full-Time
Work Mode: Remote
Hiring Locations: India, United Kingdom, Armenia, South Africa
Experience: 6+ Years (Preferred)

About the Role

Syneos Health is seeking an experienced R Statistical Programmer with strong expertise in ADaM programming, CDISC standards, and regulatory submissions. The role involves developing statistical programming deliverables, leading programming activities, supporting global clinical trials, and ensuring compliance with regulatory requirements for agency submissions.

Key Responsibilities

  • Develop programming code using R and other statistical software to generate:

    • Analysis Datasets (ADaM)

    • Tables

    • Listings

    • Figures (TLFs)

    • Regulatory Submission Deliverables

  • Perform validation programming and quality control checks.

  • Review and interpret:

    • Statistical Analysis Plans (SAPs)

    • Mock Shells

    • Programming Specifications

    • Annotated CRFs

    • Database Designs

  • Develop dataset specifications according to sponsor and regulatory requirements.

  • Ensure compliance with SOPs, Work Instructions, ICH Guidelines, and industry standards.

  • Manage multiple programming projects and timelines simultaneously.

  • Act as Lead Statistical Programmer on assigned studies.

  • Participate in sponsor meetings, kickoff meetings, and bid defense activities.

  • Provide technical mentorship and training to junior programmers.

  • Develop and maintain programming tools, macros, and standardization processes.

  • Support regulatory submission activities and inspection readiness.

  • Collaborate with Biostatistics, Data Management, and Clinical teams to ensure high-quality deliverables.

Required Qualifications

Education:

  • Bachelor's Degree in Statistics, Mathematics, Computer Science, Life Sciences, or related Scientific Discipline.

  • Equivalent programming experience may be considered in lieu of degree.

Experience:

  • Extensive experience in Statistical Programming within a Clinical Trial environment.

  • Experience leading complex or global programming projects.

  • Strong expertise in regulatory submissions and CDISC standards.

  • Experience mentoring junior programmers preferred.

Required Skills

  • R Programming

  • Statistical Programming

  • Clinical Trial Programming

  • ADaM Dataset Development

  • TLF Generation

  • CDISC Standards

  • Regulatory Submissions

  • Clinical Data Analysis

  • Validation Programming

  • SAP Review

  • Clinical Research

  • Quality Control

  • ICH Guidelines

  • Project Leadership