Senior Statistical Programmer (Contract)

• Lead and support programming deliverables for clinical studies and projects.
• Implement statistical programming aspects of study protocols and clinical development plans.
• Deliver high-quality, efficient programming outputs and ensure compliance with standards and automation tools.
• Prepare and review specifications, ensuring documentation is complete and accurate.
• Contribute to process improvement and best practice development within the programming function.
• Collaborate closely with cross-functional teams including Biostatistics, Data Management, and Project Leadership.
• Proactively identify and elevate project risks where necessary.

We are seeking an experienced Senior Statistical Programmer Consultant to support one of our key clients in the pharmaceutical industry. This is a FSP position suited to a confident professional who can work independently while fostering strong, trust-based relationships with sponsor counterparts., * Bachelor's degree in Computer Science, Statistics, or a related field with 5+ years of clinical programming (CDISC) experience, or Master's degree with 6+ years of experience.

• Proven experience in Oncology therapeutic area.
• Strong understanding of ICH/GCP guidelines, clinical trial processes, and regulatory standards.
• Solid knowledge of the drug development lifecycle and submission processes.
• Excellent communication, coordination, and stakeholder management skills.
• Demonstrated ability to manage multiple priorities and meet deadlines efficiently.