Principal Statistical Programmer Consultant - Oncology - Remote

Overview

This role focuses on delivering technical programming and information components for clinical studies, requiring high technical skills and industry knowledge.

In Short

• Work independently and establish a high-trust environment with clients.
• Lead and support programming efforts for clinical studies.
• Implement statistical programming aspects of protocols.
• Ensure high quality in deliverables.
• Write and oversee specifications and documentation.
• Contribute to best practices for quality and efficiency.
• Ensure compliance with standards and automation.
• Plan and support team activities.
• Communicate risks within projects.
• Collaborate with study team members.

Requirements

• Bachelor’s in computer science or related field with 5 years of experience; Master’s with 6 years.
• Experience in Oncology therapeutic area.
• Knowledge of ICH and Good Clinical Practices.
• Understanding of clinical drug development processes.
• Strong communication and coordination skills.
• Current knowledge of technical and regulatory requirements.
• Ability to manage concurrent project activities.
• Proficient in influencing stakeholders on programming-related items.

Benefits

• Opportunity to work directly with a single sponsor.
• Career growth opportunities within a global CRO.
• Supportive work culture focused on professional development.
• Access to training and resources for skill enhancement.
• Diversity and inclusivity in the workplace.