Senior Statistical Programmer/Analyst Consultant

📋 Description

• Support programming deliveries for a clinical study or project.
• Implements programming aspects of the protocol and development program.
• Ensure high quality in own deliverables and by other programmers.
• Programs independently with high efficiency and quality.
• Writes and oversees documentation completeness.
• Contribute to best practices to improve quality and efficiency.

🎯 Requirements

• BS in CS or statistics with 5 yrs clinical CDISC experience; MS with 6 yrs.
• Oncology therapeutic area experience.
• Strong knowledge of ICH and GCP, clinical trial process and terminology.
• Understanding of clinical drug development process.
• Strong communication and coordination skills.
• Ability to manage concurrent activities and coordinate with teams.

🎁 Benefits

• Global CRO with strong quality focus.
• Client-facing role with independence.
• Career development and training programs.
• Equal opportunity employer.