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Stat Programmer Scientist

10+ years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Education: B.Com/ BBA/ MBA/ M.Com/ B.Sc/ M.Sc/ B.Tech/ 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

Position Title:
Stat Programmer Scientist

Location:
Bengaluru, India

Employment Type:
Full Time

Job ID:
R1476381

Job Overview:
At a team, site, or staff level, the Stat Programmer Scientist provides advanced technical expertise to develop process methodologies to meet both internal and external client needs. This role involves planning and coordinating the development of integrated programming solutions across the full spectrum of statistical programming. The individual will offer technical leadership, internal consulting, and collaborate with cross-functional teams to analyze complex client or project requirements.

Key Responsibilities:

Technical Execution:

  • Plan, coordinate, and implement programming, testing, and documentation of statistical programs for complex studies.

  • Create statistical tables, listings, figures, analysis datasets, and transfer files for internal and external clients.

  • Program quality control checks for source data and periodically report data issues.

Specifications & Development:

  • Interpret complex project-level requirements and translate them into programming specifications.

  • Provide advanced technical expertise and independently propose project solutions for statistical programming challenges.

Project & Team Leadership:

  • Act as technical team lead for complex studies or a group of studies.

  • Communicate directly with internal statisticians, client statisticians, and clinical team members.

  • Ensure appropriate understanding of project requirements, and monitor and communicate project timelines and deliverables.

Resource Management:

  • Estimate scope of work and manage resource assignments.

  • Provide timely updates on project status and adjust/re-negotiate timelines as needed.

  • Promote the adoption of SOPs, best practices, and established standards.

Training & Mentoring:

  • Offer training and mentorship to statistical programming team members.

  • Help build departmental expertise and consistency in programming practices.

Required Qualifications:

Education:

  • Bachelor's Degree in Mathematics, Computer Science, Statistics, or a related field and 10 years of relevant experience required

  • OR Master’s Degree in the above disciplines and 9 years of relevant experience preferred

  • Equivalent combination of education, training, and experience will be considered

Experience & Skills:

  • Minimum 7+ years of relevant experience in statistical programming within clinical trials

  • Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language

  • Excellent understanding of statistics and the clinical drug development process

  • Strong organizational, interpersonal, and leadership skills

  • Precision and strong attention to detail

  • High-level problem-solving capabilities and mathematical aptitude

  • Advanced knowledge of data standards such as CDISC, ADaM, and SDTM

  • Ability to work collaboratively with colleagues, managers, and clients

About the Company:
IQVIA is a global leader in clinical research services, healthcare analytics, and technology solutions for the life sciences industry. Through intelligent connections, IQVIA supports innovation and accelerates the development of life-changing treatments to improve health outcomes worldwide.

Application Link:
Apply Now at IQVIA Careers