- Lead statistical design, analysis, and reporting for Phase I‑IV clinical trials
- Collaborate with clinical, regulatory, and product teams to define study objectives and statistical methodologies
- Prepare statistical analysis plans, interim and final reports, and deliverables in accordance with study protocols
- Provide independent statistical input into the development, review and submission of regulatory documentation
- Mentor junior statisticians and contribute to best practices in trial statistics
- PhD degree in Statistics, Biostatistics, or related field, and 5 years of biostatistical experience in clinical trials OR Master's degree with 8 years of experience in clinical trials
- Excellent written and oral communication skills, including technical writing and familiarity with moderate‑complex statistical methods for Phase I‑IV trials
- Proficiency in SAS, SPSS or other statistical software packages
- Strong detail orientation and ability to work on multiple tasks under tight timelines
- Proficiency in Microsoft Word and Excel
- Remote working options
- Flexible time off and paid holidays
- Medical insurance and retirement plans
- Tuition reimbursement
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Principal Biostatistician - England - Veristat

5 days ago
Description
Principal Biostatistician – Veristat
The Principal Biostatistician provides statistical input into Phase I‑IV clinical trial development, performs the analysis of clinical trial data, and contributes to the reporting of clinical trial results. The role functions as an independent lead statistician on clinical trials.
Responsibilities
Qualifications
Benefits
Veristat is an equal‑opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision‑making process.
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