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. J-18808-Ljbffr