Senior Statistical Programmer/Analyst Consultant Remote

📋 Description

• Lead/support programming deliveries for a clinical study.
• Independently perform programming tasks with high quality.
• Write and implement specifications; oversee related docs.
• Plans and supports study activities; escalate risks.
• Ensure compliance with standards and automation usage.
• Collaborate with statisticians, data managers, and leads.

🎯 Requirements

• BS in CS or Statistics or related; 5+ yrs CDISC clinical programming.
• MS in CS/Statistics or related; 6+ yrs CDISC experience.
• Oncology therapeutic area experience.
• Knowledge of ICH, GCP, regulatory terminology.
• Understanding of the clinical drug development process.
• Strong communication and coordination skills.
• Proactive in managing concurrent study activities.
• Ability to influence stakeholders on programming items.

🎁 Benefits

• Global CRO with diverse clients and projects.
• Client-facing role with independence and support.
• Focus on quality, development, and training.
• Collaborative, data-driven culture.