Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Statistical Programmer (Medical Device)

Iqvia
IQVIA
3-4 years
$88,300 – $220,900 per year
10 July 18, 2025
Job Description
Job Type: Remote 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 (Medical Device) – Remote

Job Summary:
IQVIA is hiring an experienced Statistical Programmer to support advanced programming for medical device studies. This is a fully remote opportunity, ideal for professionals with strong SAS skills and experience in CDISC standards. Join a global leader driving innovation in clinical trials and healthcare analytics.


Key Responsibilities:

  • Plan and coordinate programming for complex medical device studies.

  • Program and validate statistical tables, listings, and figures (TLFs).

  • Develop and integrate derived datasets across multiple sources/studies.

  • Create and maintain documentation including programming specifications.

  • Provide internal consulting for statistical programming solutions.

  • Lead development of new macros, technologies, and tools.

  • Serve as statistical programming team lead for studies or groups of studies.

  • Estimate workloads, manage project budgets, and support resource forecasting.

  • Train and mentor junior programming staff.


Required Skills & Qualifications:

  • Master’s in Computer Science or related field with 3+ years relevant experience, OR
    Bachelor’s degree with 4+ years of experience.

  • Proficiency in Base SAS, SAS Graph, SAS Macro Language.

  • Strong understanding of CDISC SDTM and ADaM standards.

  • Familiarity with ICH Statistical Principles for Clinical Trials.

  • Medical device experience highly preferred.

  • SAS certification preferred.

  • Solid knowledge of clinical research and statistical analysis processes.

  • Strong leadership, organizational, and communication skills.


Perks & Benefits:

  • Competitive salary range: $88,300 – $220,900 per year
    (based on experience, location, and role-specific qualifications)

  • Bonus and incentive plans

  • Comprehensive health and wellness benefits

  • Work-from-home flexibility

  • Global work environment with advancement opportunities


Company Overview:

IQVIA is a global leader in clinical research, healthcare analytics, and real-world data. We partner with top pharmaceutical and biotech companies to drive innovation, improve patient outcomes, and advance clinical development using cutting-edge technology.


Work Mode: Remote (Home-based)


Apply Today

Are you a skilled SAS programmer ready to make an impact in medical device research? Apply now to join IQVIA’s world-class statistical programming team and advance your career in clinical data science..