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Principal Biostatistician Fsp, Neuroscience

5-7 years
$115,900 – $243,900
10 Oct. 29, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Principal Biostatistician (FSP) – Neuroscience

Location: Home-based (U.S. or Canada)
Job Type: Full-time
Job ID: R1451636
Department: Data Sciences Staffing Solutions (DSSS)
Available Locations: North Carolina | Remote


About the Role

IQVIA’s Data Sciences Staffing Solutions (DSSS) provides sponsor-dedicated experts through a Functional Service Provider (FSP) model, allowing professionals to work fully embedded within top global pharmaceutical and biotech organizations.

As a Principal Biostatistician in Neuroscience, you’ll deliver statistical expertise to support the design, execution, and interpretation of innovative clinical research, helping advance the next generation of neurological therapies.


Why Join DSSS?

  • 💻 100% Home-based remote flexibility

  • ⚖️ Work-life balance with flexible scheduling

  • 🤝 Collaborate with elite, cross-functional teams in neuroscience research

  • 📈 Long-term stability and redeployment opportunities

  • 🚀 Career growth through technical training and tailored development programs

  • 💡 Focus on science and impact, not just budgets or change orders

  • 📚 Engage in regulatory submissions and cutting-edge clinical trials


Key Responsibilities

  • Partner with cross-functional teams to define project goals, statistical strategies, and timelines.

  • Author statistical sections of clinical trial protocols and statistical analysis plans (SAPs).

  • Provide oversight for programming deliverables including TLFs (Tables, Listings, Figures).

  • Conduct statistical review of study data and reports for accuracy and compliance.

  • Contribute to clinical study reports (CSRs), regulatory submissions, and exploratory analyses.

  • Support publications and scientific communications.

  • Guide and mentor statistical programmers on ADaM dataset specifications and quality checks.

  • Perform sample size/power calculations and trial simulations.

  • Review literature and validate endpoints to inform study design.

  • Apply advanced statistical methodologies such as:

    • Synthetic control arms

    • Causal inference methods

    • Rare disease modeling

    • Bayesian techniques


Qualifications

Education

  • PhD in Statistics, Biostatistics, or related field with ≥5 years industry experience
    OR

  • MS in Statistics, Biostatistics, or related field with ≥7 years industry experience

Experience & Skills

  • ≥3 years clinical trial experience (Phase II & III) + ≥2 years observational/RWE studies

  • Proficient in SAS programming and validation

  • Strong understanding of ICH GCP, ICH E9, and regulatory standards

  • Experienced in CDISC (SDTM, ADaM, CDASH)

  • Independent project management and decision-making ability

  • Strong communication and leadership skills

Preferred

  • Hands-on Neuroscience therapeutic experience


Compensation

  • 💰 Base Salary Range: $115,900 – $243,900 (annualized)

  • 💎 Additional benefits may include:

    • Incentive plans or performance bonuses

    • Comprehensive health and welfare programs

    • Long-term professional development support


About IQVIA

IQVIA is a global leader in clinical research, data science, and healthcare intelligence, dedicated to accelerating the development and commercialization of medical innovations to improve patient outcomes worldwide.

🔗 Learn more: https://jobs.iqvia.com


Equal Opportunity Statement

IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected characteristics.
🔗 Equal Opportunity Policy


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