Principal Study Statistician, Clinical Development

Scorpion Therapeutics; United States; On-site; USD 150,000 - 210,000; Full time

Job summary

Kymera Therapeutics seeks a Study/Program Lead Statistician to drive statistical efforts in clinical development. You will serve as the statistical expert on study teams, contribute to development plans, and author statistical sections for protocols and reports, while overseeing CROs and supporting regulatory submissions.

The role requires an advanced degree in statistics and at least 6 years of clinical trial experience, with expertise in SAS and familiarity with R/Python and trial design

Qualifications

• Advanced degree in Statistics or related field.
• At least 6 years of clinical trial experience in biotech/pharma.
• Expertise in SAS; familiarity with R/Python and trial design software.
• Comprehensive knowledge of FDA, EMA, and ICH guidelines.

Responsibilities

• Serve as the statistical expert on clinical study/program teams.
• Contribute to development plans; author statistical sections for protocols and reports.
• Oversee CROs and support regulatory submissions.

Skills

SAS

R/Python

Trial design software

Education

Advanced degree in Statistics or related field

Tools

SAS

Trial design software

Job description

Kymera Therapeutics seeks a Study/Program Lead Statistician to drive statistical efforts in clinical development. You will serve as the statistical expert on study teams, contribute to development plans, and author statistical sections for protocols and reports, while overseeing CROs and supporting regulatory submissions.

The role requires an advanced degree in statistics and at least 6 years of clinical trial experience, with expertise in SAS and familiarity with R/Python and trial design