Lead Statistical Programmer in Clinical Research

Step into a Lead Statistical Programmer position focused on clinical research and impactful data submission. Use your extensive TFL programming knowledge to ensure compliance with CDISC standards.
This role seeks a dedicated programmer with over six years of experience in clinical trials. You will take part in statistical programming activities and manage clinical data submissions according to established CDISC specifications. This position may also include responsibilities for project timelines and mentoring the team in best practices.
Key Responsibilities:
• Lead statistical programming for clinical trial submissions
• Develop and verify SAS programs for data analysis and conversion
• Create specifications for statistical programming documentation
• Train colleagues and support team development
• Adhere to SOPs for programming activities
Requirements:
• Minimum 6 years in statistical programming roles
• Bachelor’s in statistics, computer science, or life...