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Principal Biostatistician Fsp, Rwe

5-7 years
$131,300 – $243,900 annually
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

 

Principal Biostatistician – Real World Evidence (Remote)

Location: Remote (U.S. or Canada)
Company: IQVIA – Data Sciences Staffing Solutions (DSSS)
Job Type: Full-Time


Job Summary:

IQVIA’s DSSS (Data Sciences Staffing Solutions) unit is hiring a Principal Biostatistician to lead the statistical strategy and execution of Real World Evidence (RWE) projects. This fully remote role supports health outcomes research, epidemiological studies, and regulatory submissions, utilizing RWD sources like EMRs, claims, and registries. Ideal for experienced biostatisticians who excel in RWE analytics, SAS/R programming, and global regulatory environments.


Key Responsibilities:

  • Serve as statistical lead on RWE/HEOR/HTA projects and advise cross-functional teams

  • Design and write SAPs and protocols using RWD sources (EMR, claims, registries)

  • Select and implement statistical and ML models to support real-world research

  • Conduct cost analysis and HCRU evaluations for HTA and payer needs

  • Execute advanced analytics using SAS and R for complex RWD

  • Oversee quality control, data validation, and project timelines

  • Guide regulatory strategy for RWE submissions and publications

  • Present findings to internal and external stakeholders


Required Skills & Qualifications:

  • PhD in Statistics/Biostatistics with 5+ years industry experience OR
    MS with 7+ years in pharmaceutical/RWE analytics

  • Strong experience with claims, EMR/EHR, chart reviews, registries

  • Familiarity with LOINC, surrogate endpoints, phenotype algorithms

  • SME-level SAS skills (propensity score matching, outcome metrics)

  • Experience with R for statistical modeling and data visualization

  • Knowledge of CDISC ADaM, ICH GCP, and global HTA/RWE regulations

  • Ability to lead large multi-functional teams and complex RWE studies


Preferred (Not Required):

  • Knowledge of payer/reimbursement landscape and value frameworks

  • Exposure to regulatory and HTA submissions


Perks & Benefits:

  • Salary Range: $131,300 – $243,900 annually

  • Fully remote with flexible scheduling

  • Long-term FSP contracts with leading pharma/biotech clients

  • Comprehensive technical training and development support

  • Career growth opportunities across global therapeutic areas

  • Balanced workload with strong emphasis on team collaboration


About IQVIA:

IQVIA is a global leader in clinical research, real-world evidence, and data-driven healthcare insights. Through its DSSS division, IQVIA provides embedded talent to top-tier pharmaceutical partners, advancing patient outcomes and accelerating drug development.


Work Mode: Remote (Home-based – U.S. or Canada)


Apply Now

Are you ready to drive impactful RWE insights with world-class data? Join IQVIA’s DSSS team and help shape the future of healthcare analytics. Apply now to lead breakthrough real-world research.