Lead/Principal Statistical Programmer Consultant(Hematology/Oncology-Clinical Trials) REMOTE

Overview

The Principal Statistical Programmer Consultant will lead and support programming activities for clinical studies, requiring high technical skills and industry knowledge.

In Short

• Lead programming activities for clinical studies.
• Develop Tables, Figures, Listings (TFLs) from SAS programs.
• Customize outputs and graphics per delivery specifications.
• Ensure compliance with standards and automation.
• Contribute to best practices for quality and efficiency.
• Communicate and escalate risks within projects.
• Work independently with high efficiency and quality.
• Support programming deliveries for clinical studies.
• Plan and support team activities.
• Engage with clients to establish trust.

Requirements

• Bachelor’s or Master’s degree in CS, statistics, or related fields.
• 6-8 years of clinical programming experience.
• Experience in Oncology/Hematology TA.
• Knowledge of ICH and Good Clinical Practices.
• Strong communication and coordination skills.
• Current knowledge of technical and regulatory requirements.
• Ability to manage concurrent activities.

Benefits

• Work for a global CRO with a supportive culture.
• Opportunities for professional development.
• Engage in meaningful work contributing to healthcare.
• Be part of a diverse and inclusive team.
• Flexible working arrangements.