Job Summary
A company is looking for a Biostatistician to support drug development and regulatory submissions in a remote role.
Key Responsibilities
- Design and analyze clinical trials and contribute to the clinical development plan
- Collaborate with cross-functional teams to deliver statistical components for trials and submissions
- Lead and monitor statistical activities across multiple clinical trials
Required Qualifications
- 5+ years of relevant experience in biostatistics
- Strong expertise in drug development and clinical trials
- 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
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