Instagram
youtube
Facebook

Stat Programmer Scientist

7+ years
Not Disclosed
10 Dec. 19, 2024
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

Job Title: Senior Statistical Programming Lead
Location: [Insert Location]
Job Type: Full-Time

Job Overview:
Provide advanced technical expertise to develop process methodology that meets internal and external client needs. Plan and coordinate the development of integrated programming solutions, covering the full spectrum of statistical programming requirements. Offer technical leadership and internal consulting services, including specifications and user needs analysis for complex projects or client requirements.

Essential Functions:

  • Plan, coordinate, and implement the programming, testing, and documentation of statistical programs for complex studies, including statistical tables, figures, listings, and derived datasets.
  • Develop programming specifications for complex studies and interpret project-level requirements.
  • Provide advanced technical expertise for internal and external clients and independently offer project solutions.
  • Lead technical teams for single or multiple complex studies.
  • Communicate directly with internal statisticians and clinical teams to ensure a clear understanding of requirements and timelines.
  • Estimate programming scope, manage resource assignments, and adjust timelines as necessary.
  • Promote the use of established standards, SOPs, and best practices.
  • Mentor and train team members within the Statistical Programming department.

Qualifications:

  • Bachelor's Degree in Maths, Computer Science, Statistics, or related field with 4+ years of relevant experience, or
  • Master's Degree in Maths, Computer Science, Statistics, or related field with 3+ years of relevant experience.
  • Typically requires 7+ years of prior relevant experience.
  • Advanced knowledge of statistics, programming, and clinical drug development processes.
  • Proficiency in Base SAS, SAS Graph, and SAS Macro Language.
  • Expertise in Data Standards such as CDISC, ADaM, and SDTM.
  • Excellent organizational, leadership, communication, and interpersonal skills.
  • Strong attention to detail and problem-solving aptitude.

Company Overview:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. We accelerate the development and commercialization of medical treatments to improve patient outcomes worldwide.

Job Function: Statistical Programming
Role: Full-Time