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Your Role:
- Provide consulting on statistics activities for clinical trials, acting as study statistician.
- Develop and finalize statistical analysis plans, randomization schedules, and study-specific deliverables.
- Ensure quality control of statistical programming outputs and mentor team members.
Qualifications:
- Master in Statistics or Biostatistics preferred; SAS certification is a plus.
- 10+ years in pharmaceutical/biotechnology industry or equivalent statistical consulting role.
- Strong knowledge of ICH, GCP, 21 CFR Part 11, CDISC standards, and clinical reporting processes.
What We Offer:
- Opportunity to accelerate your skills and career in a fast-growing company.
- A people-first, inclusive culture with recognition for remote work excellence.
- Engagement in meaningful work impacting the future of healthcare.
Eclinical Solutions
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. It is a fast-growing company that has won the 2025 Top Workplaces USA Award for Remote Work and emphasizes an inclusive culture and work-life balance.