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Sr Stat Programmer

7+ years
Not Disclosed
10 Jan. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Title: Senior Statistical Programmer

Job Description Overview:
As a Senior Statistical Programmer at IQVIA, you will provide advanced technical expertise to develop programming solutions for complex studies, serving both internal and external clients. You will plan, coordinate, and execute statistical programming activities, ensuring quality control and compliance with project requirements. This role involves leading technical teams, collaborating with statisticians and clinical teams, and mentoring junior staff.

Essential Functions:

  • Perform and coordinate programming, testing, and documentation of statistical programs for complex studies, including statistical tables, figures, listings, and derived datasets.
  • Develop specifications and programming solutions for complex studies, ensuring accurate and timely delivery of analysis datasets and transfer files.
  • Provide advanced technical leadership, identifying solutions to complex challenges and communicating these with internal and external teams.
  • Manage project timelines, resource assignments, and scope of work, ensuring quality deliverables.
  • Directly collaborate with statisticians and clinical teams to align on requirements and timelines.
  • Promote the use of established standards, SOPs, and best practices within the department.
  • Provide training and mentorship to statistical programming team members.

Qualifications:

  • Bachelor's Degree in Maths, Computer Science, Statistics, or related field with 8 years of relevant experience required. Or
  • Master's Degree in Maths, Computer Science, Statistics, or related field with 7 years of relevant experience preferred.
  • Requires 7+ years of prior relevant experience.
  • Advanced knowledge of statistical programming, clinical drug development, and relevant data standards such as CDISC/ADaM/SDTM.
  • Proficiency in SAS, including Base SAS, SAS Graph, and SAS Macro Language.
  • Excellent organizational, leadership, and communication skills.
  • Strong attention to detail and problem-solving abilities.

About IQVIA:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, dedicated to improving patient outcomes through innovative medical treatments. Learn more about our work and opportunities at IQVIA Careers.