Principal Statistical Programmer

Responsibilities:

• Responsible for supporting the Programming deliveries of a clinical study or project.
• Implements statistical programming aspects of the protocol and the clinical development program
• Ensures high quality is built into own deliverables and the quality delivered by other programmers
• Programs independently with high efficiency and quality
• Writes and/or implements specifications and oversees completeness of relevant documentation
• Contribute to the development of best practice to improve quality, efficiency and effectiveness within function
• Ensures compliance with standards and automation usage
• Plans and support team activities and tasks
• Communicates and escalates risks within the assigned studies and/or projects
• Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.

Requirements:

• Bachelor's degree in computer science (CS), statistics or related scientific disciplines with 7 yrs. clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 5 yrs. of clinical programming (CDISC) experience.
• Require strong Oncology TA with experience in ISS & Client.
• Experience in blood cancer and the Lugano criteria is a plus.
• Excellent programming skills including macro language.
• Ability to proactively manage concurrent activities within a study or part of project.
• Proficient knowledge of the clinical development process.