Planning and working with the clinical programming group to schedule specification, programming, validation and ongoing delivery activities. Ability to write and execute SAS programs to produce internal and Sponsor deliverables. Leads timelines for programming setup process, ensuring issues are addressed and producing clinical data delivery validation packages to the study teams to file in the Trial Master File. Participates in activities related to the specification review, program validation and quality assurance of study data deliverables, applying expert experience and knowledge to support the clinical data programmers assigned to a clinical study. Attends sponsor audits, including presenting the Clinical Data Delivery process and procedures from a compliance perspective. You will need: Degree in a Technical or Science background coupled with strong experience in Clinical Data Management and SAS programming. Ability to work to tight deadlines and effectively run multiple projects to specific client requests. Strong communication skills as you will be working across a highly matrix organization internally and externally.
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