Responsibilities

• Develop and implement statistical analysis plans for clinical trials.
• Collaborate with cross-functional teams to design studies and analyze data.
• Provide statistical guidance and support to project teams throughout the study lifecycle.
• Ensure compliance with regulatory standards and internal policies.
• Prepare and review statistical reports, presentations, and publications.
• Utilize statistical software to perform complex data analyses and visualizations.
• Mentor junior statisticians and contribute to their professional development.

Requirements

• Master's degree or Ph.D. in Statistics, Biostatistics, or a related field.
• 5+ years of experience in a statistical role within clinical research.
• Proficiency in statistical software (e.g., SAS, R, or equivalent).
• Strong understanding of clinical trial design and analysis methodologies.
• Excellent communication skills and ability to work collaboratively in a team environment.
• Detail-oriented with strong problem-solving skills.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance plans.
• Flexible working hours and remote work options.
• Generous vacation and paid time off policies.
• Opportunities for professional development and career advancement.
• A supportive and inclusive work environment that values diversity.