Principal Statistician
Listed on 2026-01-14
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Science
Data Scientist, Clinical Research, Research Scientist, Medical Science
Position: Principal Statistician
FLSA Status: Exempt
Location: Hybrid (Somerset, NJ)
Salary: $110,000 to $135,000 per year
Company Overview: Pharmaron is a global contract research organization that supports pharma and biotech companies from discovery through manufacturing with fully integrated, high‑quality services. With over 21,000 employees worldwide across 23 locations in the US, UK, and China, we have delivered 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases.
Job Overview- Develop and/or review statistical sections of a study protocol with high complexity independently.
- Perform and/or verify sample size and statistical power calculations for typical trial designs.
- Develop statistical analysis plans, table/listing/figure mock‑ups, and statistical analysis reports for studies of varying complexity.
- Act as a randomization statistician to develop the randomization protocol and generate the randomization schedule.
- Attend client meetings, including project kick‑off meetings, resource/timeline discussions, bid defenses, and blind data review meetings.
- QC/review case report forms and other DM documents such as edit check specifications, data review plans, data transfer specifications, etc.
- QC/review programming deliverables, including programming specifications, analysis datasets, and TLFs, ensuring analysis requirements are met.
- Mentor statistical programmers on statistical design and model implementation.
- Mentor biostatisticians on relevant statistical work.
- Ensure all activities comply with internal and external quality standards, SOPs/WIs, ICH‑GCP, and applicable local and international regulations, guidelines, and industry standards.
- Master’s degree or higher in biostatistics, statistics, mathematics, or a related discipline; a bachelor’s degree with equivalent experience may be considered.
- 5+ years of relevant experience in clinical trial statistics.
- Proficiency with SAS Base, SAS/Macros, SAS/Graph, SAS/Stat, and the reporting process.
- Familiarity with CDISC CDASH/SDTM/ADaM standards.
- Compliance with SOPs/WIs, ICH‑GCP, and other relevant regulations and guidelines.
- Medical, Dental & Vision insurance with significant employer contributions.
- Employer‑funded Health Reimbursement Account.
- Healthcare & Dependent Care Flexible Spending Accounts.
- 100% employer‑paid employee life and AD&D insurance, short‑ and long‑term disability insurance.
- 401(k) plan with generous employer match.
- Access to an Employee Assistance Program. >
How to Apply
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and affirmative action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed.
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology
Industries: Pharmaceutical Manufacturing
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