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Principal Stat Programmer

5+ years
Not Disclosed
10 May 20, 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

Job Title: Principal Statistical Programmer
Location: Bengaluru, India
Job ID: R1483940
Job Type: Full-time
Job Available in Additional Locations


Job Description:

IQVIA is seeking a highly experienced and skilled Principal Statistical Programmer to join its dynamic team. The ideal candidate will have strong expertise in clinical data programming, with deep knowledge of advanced data structures, regulatory submission standards, and programming tools used in clinical trial data analysis and reporting. This is a critical role that supports the planning and execution of clinical data processing, statistical analysis, and submission deliverables.


Key Responsibilities:

  • Design, develop, and maintain statistical programs for clinical studies, ensuring adherence to regulatory and company standards.

  • Apply in-depth knowledge of data structures and relevant programming languages (SAS, SQL, Python, R) for data manipulation, integration, and reporting.

  • Work with complex and diverse data types, including biomarkers, ECG, imaging, and digital health data, to derive meaningful insights.

  • Transform vendor-supplied data into SDTM-compliant datasets; experience with Define.xml, CDASH, and metadata is highly desirable.

  • Apply knowledge of ADaM standards and statistical analysis methodologies in clinical trial submissions.

  • Utilize tools such as Spotfire, Tableau, Qlik, JReview, Business Objects, Oracle BI, etc., to create dashboards, support clinical data review, and facilitate analytics and visualization.

  • Collaborate with cross-functional teams including biostatistics, clinical data management, and regulatory affairs to ensure quality and timely deliverables.


Qualifications:

  • Minimum Experience: 5+ years in statistical programming within the clinical research or pharmaceutical industry.

  • Programming Skills: Proficient in SAS; additional experience with SQL, Python, or R preferred.

  • Standards Knowledge: Deep understanding of SDTM, CDASH, Define.xml, and metadata; ADaM experience is a plus.

  • Data Handling: Strong grasp of handling and transforming complex clinical data types including digital health sources.

  • Visualization Tools: Familiarity with analytics and reporting tools such as Spotfire, Tableau, and Oracle BI.

  • Soft Skills: Excellent analytical, problem-solving, and communication skills with the ability to work collaboratively in cross-functional environments.


About IQVIA:
IQVIA is a global leader in healthcare intelligence, clinical development, and advanced analytics. We drive innovation in medical research and healthcare delivery by combining data, technology, and expertise to accelerate the creation of better treatments and improved patient outcomes. Learn more at
IQVIA Careers.