Responsibilities

• Develop and oversee study protocols, including design, sample size calculations, randomization, and statistical analysis plans for assigned projects.
• Provide comprehensive statistical oversight to ensure quality and consistency with project requirements.
• Ensure data integrity and completeness for all statistical analyses, maintaining high standards of accuracy and consistency.
• Prepare statistical analysis plans and guarantee the accuracy and timely delivery of statistical contributions to reports and decisions.
• Validate analyses and ensure compliance with regulatory requirements throughout the study lifecycle.

Requirements

• Master's or Ph.D. in Statistics, Biostatistics, or a related field.
• Proven experience in a similar role within the clinical research or pharmaceutical industry.
• Strong knowledge of statistical methodologies and software (e.g., SAS, R).
• Exceptional communication skills, with a capability to work collaboratively in a client-facing environment.
• Ability to work independently and manage multiple projects simultaneously in a remote setting.

Benefits

• Competitive salary and performance-based bonuses.
• Flexible working hours and the possibility of remote work.
• Comprehensive health benefits package.
• Opportunities for professional growth and development.
• A supportive and inclusive work culture that values diversity.