Senior Statistical Programmer/Analyst Consultant

📋 Description

• Delivery-focused programming lead for a clinical study.
• Leads/assists programming efforts under team leadership.
• Delivers high-quality outputs and ensures quality across others.
• Programs independently with efficiency and accuracy.
• Collaborates with study team and communicates risks.

🎯 Requirements

• Bachelor’s in CS or stats with 5+ CDISC programming years; Master’s with 6+.
• Oncology TA experience.
• Knowledge of ICH/GCP, clinical research, regulatory terms.
• Strong communication and coordination skills.
• Understanding of clinical drug development process.
• Ability to plan, coordinate, and manage concurrent tasks.

🎁 Benefits

• Global CRO with focus on quality and growth.
• Client-facing role with high-trust environment.
• Opportunities for professional development and training.
• Equal opportunity employer promoting diversity.