Job Search and Career Advice Platform

Enable job alerts via email!

Principal Statistical Programmer Lead - Remote

Parexel International

Remote

USD 90,000 - 130,000

Full time

Today
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A global clinical research organization is seeking a Principal Statistical Programmer to lead statistical programming teams and ensure high-quality, regulatory-compliant deliverables across clinical studies. The ideal candidate will have advanced SAS programming expertise and strong analytical skills. Responsibilities include developing SDTM and ADaM datasets, leading project teams, and mentoring junior staff. This remote role offers a full-time position and is ideal for innovative individuals with a strong background in clinical trials.

Qualifications

  • Strong command of written and spoken English.
  • Experience supporting clinical trials across therapeutic areas is highly desirable.

Responsibilities

  • Serve as Statistical Programming Lead on assigned projects.
  • Lead programming teams to deliver high-quality outputs.
  • Develop and QC SDTM, ADaM datasets and analysis outputs.

Skills

Advanced SAS programming expertise
Analytical and problem-solving skills
Understanding of clinical programming standards
Project management capabilities
Excellent organizational skills
Communication skills
Mentoring skills

Education

Bachelor’s degree in Statistics, Computer Science, Mathematics or Life Sciences
Job description
A global clinical research organization is seeking a Principal Statistical Programmer to lead statistical programming teams and ensure high-quality, regulatory-compliant deliverables across clinical studies. The ideal candidate will have advanced SAS programming expertise and strong analytical skills. Responsibilities include developing SDTM and ADaM datasets, leading project teams, and mentoring junior staff. This remote role offers a full-time position and is ideal for innovative individuals with a strong background in clinical trials.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.