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Sr Statistical Programmer

5+ years
Not Disclosed
10 April 11, 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: Senior Statistical Programmer
Location: Home-Based, India (Asia Pacific)
Company: Syneos Health
Job ID: 25002282


Job Overview:

Syneos Health is hiring a Senior Statistical Programmer to lead and execute clinical trial programming using SAS. This role involves advanced statistical programming, quality assurance, leadership in projects, and client interaction — all within a dynamic, remote work environment.


Why Join Syneos Health?

  • Join a global team of 29,000+ employees across 110 countries

  • Work on FDA- and EMA-approved products and high-impact clinical trials

  • Experience a Total Self culture that supports individuality and inclusion

  • Grow your career with continuous development, mentoring, and technical training

  • Be part of a company where your work truly matters


Key Responsibilities:

  • Write SAS code to create summary tables, data listings, graphs, and derived datasets per SAP/specifications

  • Perform validation programming and resolve findings with team members

  • Maintain accurate and complete project documentation for inspection readiness

  • Manage timelines, reprioritize as needed, and align goals with management

  • Lead programming tasks and support multiple projects simultaneously

  • Write detailed specifications for complex datasets and outputs

  • Conduct and lead effective internal and sponsor meetings

  • Review SAPs, mock shells, CRFs, database design, and provide actionable feedback

  • Mentor junior programmers and review work of SP1 team members

  • Participate in bid defenses, kickoffs, and client discussions

  • Conduct 2nd-level Manual QC of outputs, CSR-TLF document comparisons, and project management tasks


Required Qualifications:

  • Bachelor’s degree in statistics/scientific discipline or equivalent experience

  • 5+ years of SAS programming in a clinical trial environment

  • Proficiency in:

    • Base SAS, Macros

    • SDTM & ADaM dataset generation

    • TLF creation

  • Strong attention to detail and critical thinking

  • Effective communication and client interaction skills

  • Ability to handle project planning, task negotiation, and timelines

  • Fluent in spoken and written English


Additional Information:

  • Job responsibilities are not exhaustive and may be modified as needed

  • The role is compliant with global equality and disability directives

  • No employment contract is implied