Biostatistician
Resource1
- Parsippany, NJ
- Permanent
- Full-time
- Collaborate with cross-functional teams to design and implement statistical methodologies for clinical trials, including sample size determination, randomization schemes, and statistical analysis plans
- Analyze and interpret data using appropriate statistical techniques, ensuring the accuracy, validity, and reliability of results
- Develop and validate statistical models to support clinical study endpoints including regression analysis, and longitudinal data analysis
- Provide statistical input in the development and review of study protocols, method validations, and other study-related documents
- Generate statistical analysis reports, presenting findings to internal and external stakeholders in a clear and concise manner
- Contribute to the continuous improvement of statistical practices within the organization by staying current with advances in biostatistics methodologies
- Collaborate with researchers to ensure compliance with regulatory requirements and industry standards
- Master's degree in Biostatistics, Statistics, or a related field
- At least 5 years demonstrated experience using statistical software such as SAS, R, or Python
- At least 3 years working with statistics and data to generate a variety of results
- Proven experience in applying statistical methods in a clinical research setting, preferably within the pharmaceutical or biotechnology industries
- Solid understanding of clinical trial design, protocols, and regulatory requirements
- Possess strong analytical skills with the ability to solve complex problems and make sound decisions based on statistical analysis