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Statistical Programmer I - Pune (Office- Based)

1-2 years
Not Disclosed
10 March 28, 2025
Job Description
Job Type: Full Time 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

Statistical Programmer I – Pune (Office-Based)
Location: India, Asia Pacific – IND-Home-Based
Job ID: 25002281
Updated: Today

About Syneos Health:
Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. We combine clinical, medical affairs, and commercial insights to drive outcomes aligned with modern market realities.

Our Clinical Development model places the customer and the patient at the center of our operations, continuously striving to simplify and streamline processes to make Syneos Health not only easier to work with but also easier to work for. Whether in a Functional Service Provider (FSP) partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, working as a team to help customers achieve their goals.

Why Syneos Health?

  • We have worked with 94% of all Novel FDA Approved Drugs over the last 5 years.

  • 95% of EMA Authorized Products have involved Syneos Health.

  • We’ve conducted over 200 Studies across 73,000+ sites and engaged 675,000+ trial patients.

Job Responsibilities:

  • Use SAS or other software to generate summary tables, data listings, graphs, and derived datasets per statistical analysis plans and programming specifications.

  • Ensure that outputs meet quality standards and project requirements.

  • Perform validation programming and collaborate with Statistical Programmers, Biostatisticians, and project team members to resolve discrepancies or findings.

  • Maintain well-organized, complete, and up-to-date project documentation, including verification/quality control documents and programs, ensuring inspection readiness.

  • Manage scheduling and time constraints across multiple projects, setting goals based on priorities from management, and adjusting to timeline or priority changes effectively.

  • Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for others’ opinions.

  • Display willingness to collaborate and assist with projects and initiatives to meet business needs.

  • Complete project programming activities within the timeframe allotted by the Lead Statistical Programmer and/or management.

  • Perform other work-related duties as assigned.

  • Minimal travel may be required.

Qualifications:

  • Education: Undergraduate Degree in a scientific or statistical discipline preferred. In lieu of a degree, an equivalent combination of education and demonstrated programming experience will be considered.

  • Experience: 6 months to 2 years of experience in a related field.

  • Programming Skills: Proficiency in SAS or other relevant software, preferably in a clinical trial environment.

  • Critical Skills:

    • Attention to detail with strong analytical and critical thinking abilities.

    • Understanding of clinical domain concepts.

    • Quality Control (QC) of outputs and programming activities.

  • Communication Skills: Excellent written and verbal communication in English.

Additional Information:
Tasks, duties, and responsibilities listed in this job description are not exhaustive. Syneos Health may assign other duties as required, and qualifications may differ based on company discretion. Syneos Health is an equal opportunity employer and complies with all applicable laws, including the Americans with Disabilities Act, ensuring reasonable accommodations where necessary.