Biostatistician

About the Role

Our client is seeking a skilled and analytical Biostatistician to join their clinical development team in Sheffield . You will be responsible for designing statistical analysis plans, performing complex statistical analyses of clinical trial data, and contributing to regulatory submissions. This role is crucial for ensuring the scientific integrity and interpretability of study results. You will work closely with clinical researchers, data managers, and medical writers to translate data into actionable insights, supporting the successful development and approval of new pharmaceutical products.

Key Responsibilities

• Design statistical analysis plans (SAPs) for clinical trials.
• Perform statistical analyses using SAS or R, ensuring accuracy and adherence to protocols.
• Interpret statistical results and contribute to clinical study reports (CSRs) and publications.
• Collaborate with clinical teams to define study designs and data collection requirements.
• Ensure statistical methodologies comply with regulatory guidelines (e.g., FDA, EMA).

Requirements

• Master's or Ph.D. in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 3 years of experience as a biostatistician in the pharmaceutical or biotech industry.
• Proficiency in statistical software such as SAS or R.
• Strong understanding of clinical trial design and methodologies.
• Excellent communication and collaboration skills.

Benefits

• Competitive salary and performance-based incentives.
• Opportunity to work on diverse and impactful clinical development projects.
• Comprehensive health and wellness benefits.
• Retirement savings plan with company match.
• Professional development opportunities and conference attendance.