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Sr Statistical Programmer(Early Phase)

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: Senior Statistical Programmer


Company: Syneos Health®

Location: India (Home-Based)

Department: Statistical Programming

Updated Date: Not specified (based on job content recency: 2025)


About Syneos Health:

Syneos Health® is a fully integrated biopharmaceutical solutions company with a global footprint of 29,000 employees across 110 countries. Focused on accelerating customer success, the company blends clinical, medical, and commercial insights to drive innovation and deliver outcomes. Their collaborative culture centers around the “Total Self” philosophy—empowering employees to bring their whole selves to work.


Why Join:

  • Career development opportunities

  • Inclusive, diverse, and supportive workplace

  • Peer recognition and total rewards program

  • Exposure to industry-leading clinical trials (94% of all FDA Novel Drug Approvals, 95% of EMA Products in the last 5 years)


Job Responsibilities:

  • Develop custom SAS (or equivalent) code for generating TLFs and datasets per specifications

  • Ensure quality outputs meeting regulatory and project standards

  • Perform validation programming and resolve issues with cross-functional teams

  • Maintain accurate, complete, and inspection-ready documentation

  • Lead statistical programming for assigned projects and direct junior programmers

  • Review key documentation: SAPs, mock shells, specifications, CRFs, database designs

  • Participate in sponsor-facing meetings (e.g., bid defenses, kickoffs)

  • Anticipate and solve programming issues, define dataset variables, and optimize efficiency

  • Conduct internal meetings, manage timelines, and provide progress updates

  • Assist in mentoring, training, and peer review activities

  • Perform delivery transfers and other assigned tasks

  • Minimal travel may be required


Qualifications:

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

  • Strong SAS or similar programming experience in a clinical trial environment

  • Understanding of clinical trial processes and programming documentation

  • Excellent verbal and written English communication skills


Additional Information:

  • Responsibilities may evolve without prior notice

  • Equivalent education/experience will be considered

  • Role complies with global employment laws and ADA (reasonable accommodations provided)