Senior Statistical Programmer/Analyst Consultant

📋 Description

• Supports programming deliveries of a clinical study or project.
• Implements programming aspects of the protocol and development program.
• Ensures high quality in own deliverables and other programmers.
• Programs independently with high efficiency and quality.
• Writes/implements specifications and oversees relevant documentation.
• Plans and supports study team activities and tasks; Escalates risks.

🎯 Requirements

• Bachelor’s in CS/statistics with 5+ years CDISC clinical programming.
• Master’s in CS/statistics with 6+ years CDISC clinical programming.
• Oncology TA experience.
• Knowledge of ICH/GCP, clinical research, regulatory requirements.
• Understanding of the clinical drug development process.
• Strong communication and coordination skills; stakeholder influence.

🎁 Benefits

• Global CRO with focus on quality and development.
• Professional development and supportive culture.
• Equal opportunity employer with emphasis on diversity.