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Clinical Trial Design
Position Overview:
- Provide advanced statistical expertise and scientific leadership within a collaborative biometrics and data science environment.
- Support complex clinical research projects across multiple therapeutic areas, transforming data into meaningful insights.
- Contribute to study design, statistical analysis, and regulatory-quality deliverables.
Key Responsibilities:
- Lead statistical analysis planning, methodology development, and interpretation of complex clinical data.
- Author and review Statistical Analysis Plans, TLFs, and ADaM datasets.
- Mentor colleagues and promote best practices in statistical methodology and governance.
Requirements:
- Advanced degree in Biostatistics, Statistics, or a related quantitative discipline.
- 7+ years of experience as a Statistician in a CRO, pharmaceutical, or biotechnology environment.
- Strong programming skills in SAS; experience with R is a plus.
Benefits:
- Fully remote work environment with flexible working hours.
- Career development opportunities, mentorship, and continuous learning support.
- Collaborative and supportive culture focused on technical excellence and innovation.
Partner Company
The partner company provides advanced statistical expertise and scientific leadership within a collaborative biometrics and data science environment, supporting complex clinical research projects across multiple therapeutic areas. The company fosters a collaborative and supportive culture focused on technical excellence and innovation, with a team of experienced professionals.