1357# Senior Statistical Programmer Consultant (Remote in Poland)

Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience Oncology TA experience Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology Good understanding of the clinical drug development process Strong communication skills and coordination skills Current knowledge of technical and regulatory requirements relevant for the role Ability to proactively manage concurrent activities within a project Proficient ability to influence relevant stakeholders on programming-related items

Support Programming deliveries of a clinical study or project. Implement statistical programming aspects of the protocol and clinical development program. Ensure high quality in own deliverables and those of other programmers. Program independently with high efficiency and quality. Write and/or implement specifications and oversee documentation completeness. Contribute to the development of best practices. Ensure compliance with standards and automation usage. Plan and support team activities and tasks. Communicate and escalate risks within assigned studies/projects. Work proactively with study team members.