Senior Statistical Programmer

This is a fully remote position, open to applicants in United Kingdom, +4 more states.

📋 Description

• Analyze clinical trial data and assist in the statistical analysis process to guarantee high-quality outcomes.

• Lead statistical programming initiatives that require technical expertise, emphasizing quality and ongoing improvement.

• Create and validate SAS programs for the statistical analysis and reporting of clinical trial data.

• Collaborate with biostatisticians to establish analysis plans and statistical methods for clinical data.

• Conduct quality control checks on statistical outputs, ensuring accuracy and consistency in reporting.

• Aid in the preparation of statistical reports, presentations, and publications for regulatory submissions.

• Contribute to enhancements in processes by identifying efficiencies in programming practices and methodologies.

⛳️ Requirements

• Bachelor's degree in statistics, computer science, mathematics, or a related field.

• Experience in statistical programming, ideally within a clinical research or pharmaceutical environment.

• Strong expertise in SAS programming.

• Solid comprehension of statistical concepts and methodologies.

• Excellent analytical and problem-solving abilities.

• Strong attention to detail.

• Effective communication skills.

• Ability to work collaboratively in a team setting.

• Capable of effectively conveying complex information.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs that include medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Learning and development opportunities through structured training and career pathways.

• Reasonable accommodations during the recruitment process.