Job Summary
A company is looking for a Biostatistician to design and analyze clinical trials in a remote setting.
Key Responsibilities
- Design and analyze clinical trials, contributing to the clinical development plan
- Collaborate with cross-functional teams to deliver statistical components for clinical trials and regulatory submissions
- Lead and monitor statistical activities across multiple clinical trials while ensuring compliance with guidelines and standards
Qualifications
- 5+ years of relevant experience in biostatistics and drug development
- Proficiency in statistical software such as SAS and/or R
- Experience with regulatory submissions and knowledge of eCRT and Define standards
- Masters or PhD in Statistics or a related field
- Preferably experienced in Immunology and modern statistical models
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