Principal Statistical Programmer - Late Phase Clinical - Remote

Overview

As a Principal Statistical Programmer, you will lead programming activities in late-phase clinical trials focusing on Cardiovascular, Renal, and Metabolism (CVRM), ensuring high-quality deliverables and compliance with industry standards.

In Short

• Lead programming delivery for CVRM projects.
• Implement statistical programming for clinical protocols.
• Ensure high quality of project deliverables.
• Drive best practices in programming.
• Manage risks in complex projects.
• Provide expert guidance to project teams.
• Ensure compliance with regulatory requirements.
• Mentor junior programming staff.
• Contribute to process improvement initiatives.
• Maintain expertise in industry standards.

Requirements

• Bachelor’s degree in Computer Science, Statistics, or related field.
• 8+ years of SAS programming experience.
• Experience with CDISC standards.
• Knowledge of ICH and GCP.
• Strong understanding of clinical drug development.
• Excellent communication skills.
• Proficient in risk management.
• Ability to influence stakeholders.
• Experience in leading cross-functional teams.

Benefits

• Work for a global CRO with a supportive culture.
• Opportunities for professional development.
• Engage in meaningful work in drug development.
• Collaborate with diverse teams globally.
• Contribute to a healthier and safer world.