Clinical Statistical Programmer with SAS Expertise

Advance your career with a leading clinical trials team as a Senior Statistical Programmer. Utilize your extensive SAS skills and CDISC knowledge to enhance data submission processes effectively.
With over six years in statistical programming, this role allows you to leverage your expertise in TFL programming while supporting vital clinical trials. You will play an essential part in ensuring submission readiness, enhancing data quality, and may lead project management tasks, focusing on timeliness and resource distribution.
Key Responsibilities:
• Prepare clinical data submissions adhering to CDISC standards
• Develop and validate SAS programs for data analysis
• Provide training and mentorship to statistical programming staff
• Create detailed programming specifications for diverse data types
• Maintain compliance with Standard Operating Procedures (SOPs)
Requirements:
• At least 6 years of statistical programming experience
• Bachelor’s degree in statist...