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Stat Programmer

7-8 years
Not Disclosed
10 July 16, 2025
Job Description
Job Type: Hybrid 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 – SAS | Hybrid (Hyderabad)

Location: Hyderabad, India
Job Type: Full-time
Work Mode: Hybrid
Salary Range: Not specified


Job Summary

IQVIA is looking for a Statistical Programmer with strong SAS expertise and leadership capabilities to join its clinical research programming team in Hyderabad. This role involves providing technical direction and oversight for statistical programming deliverables across global clinical trial projects. Ideal for experienced professionals in statistical programming for the pharmaceutical industry, the position offers the opportunity to lead a team and contribute to high-impact healthcare projects.


Key Responsibilities

  • Serve as the lead statistical programmer on clinical trials (Phase I–IV)

  • Provide advanced technical consultation on statistical programming methods

  • Review and enhance processes for programming standards and validation

  • Mentor, coach, and manage a team of statistical programmers

  • Monitor project status, timelines, and team utilization

  • Lead or support bid defenses, project kick-off meetings, and client interactions

  • Collaborate with global project leads to manage staffing, workloads, and technology needs

  • Ensure quality delivery of SAS programming outputs for statistical analysis

  • Participate in audits, inspections, and training initiatives


Required Skills & Qualifications

  • Master’s in Computer Science or related field with 7+ years of relevant experience including 1+ year in a leadership role
    OR
    Bachelor’s with 8+ years experience and 1+ year in leadership

  • Advanced SAS programming skills; experience with clinical trial datasets

  • Strong knowledge of statistical methods and CDISC standards

  • Experience in managing multiple clinical trial projects and competing priorities

  • Proficiency in project finance concepts such as EAC, forecasting, and budget burn rates

  • Excellent communication, leadership, and mentoring skills

  • Experience in client engagement, proposal support, and team development


Perks & Benefits

  • Work on high-impact global clinical trials

  • Leadership role within a globally recognized healthcare organization

  • Hybrid working model with flexibility

  • Opportunities for upskilling, mentorship, and professional growth

  • Exposure to regulatory audits and industry-leading technology platforms


Company Description

IQVIA is a world leader in healthcare analytics, clinical research, and technology solutions. With over 82,000 professionals globally, IQVIA is driving innovation to improve healthcare delivery and advance patient outcomes through powerful data and tech capabilities.


Work Mode

Hybrid – Based in Hyderabad with flexible remote collaboration.


Call to Action

Ready to lead global clinical programming initiatives in a high-growth healthcare setting? Apply now to join IQVIA as a Statistical Programmer and help transform clinical research with data-driven insights.