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.
https://www1.jobdiva.com/candidates/myjobs/openjob_outside.jsp?a=irjdnw4aqkb0a5bhkjucv8p00hyqhk05031z6ahtakm0pgjg8f34dc29wtyqerjr&from=COMP&id=11795527&SearchString=&StatesString=&jobseq=3&rowsperpage=30&divisions=&divisions2=
No comments:
Post a Comment