Roles and Responsibilities : Lead statistical programming activities as Trial Programmer for 1-2 studies or assigned project level activities. If assigned to cross-project aligned group (e.g. Standards), manage at least one, macro/utility function or local project. Co-ordinate activities of all programmers either internally or externally (FSP, CRO) assigned to the study/studies. Make statistical programming recommendations at study level. Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope), e.g. as member of the Clinical Trial Team. Review eCRF, discuss data structures and review activities as member of the Data Review Team.
https://www.indeed.com/viewjob?t=clinical+sas+programmer&jk=3acea5f440cf492f&_ga=2.144371829.1199380306.1551993568-2077807285.1533320279
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