Manager, Statistical Programming (remote)

📋 Description

• Lead and support programming for clinical studies and regulatory submissions.
• Develop TFLs from existing SAS programs, or create new outputs.
• Independently program and review reports and outputs.
• Customize outputs for target audience under biostatistician guidance.
• Support programming deliveries for a study or project.
• Plan and support team activities; communicate and escalate risks.

🎯 Requirements

• Bachelor’s in CS/statistics with 6+ yrs CDISC; Master’s with 8+ yrs.
• Oncology/Hematology TA experience.
• ISS and ISE experience.
• ICH/GCP, clinical trial process, and regulatory knowledge.
• Strong communication and coordination skills.
• Ability to proactively manage concurrent activities within a project.

🎁 Benefits

• Remote work in a client-facing role with a global CRO.
• Focus on quality and professional development in a supportive culture.
• Opportunities to work across the Americas, Europe, and Asia-Pacific.
• Ongoing training and development.
• Equal opportunity employer.