Job Description :
Senior Statistical Programmer - SDTM
Location: Remote U.S.
*Strong focus will be on SDTM experience*
BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, or work experience equivalent
Greater than 5 years of relevant career experience programming in a clinical development environment
Excellent SAS data manipulation, analysis and reporting skills
Ability to provide quality output and deliverables
Ability to write, test, and validate SAS programs, and review resulting output and data.
Excellent oral and written English communication skills
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
Good knowledge of Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) standards and the principles on which it is founded
Ability to work effectively and successfully in a team environment
Ability to manage challenging timelines
Willingness and ability to learn and follow standard processes and procedures
Ability to work effectively on multiple tasks or projects
Ability to effectively perform complex statistical programming and related tasks
Willingness and ability to provide guidance to team members on technical and process questions
Responsibilities for this role involves, but not limited to, data manipulation, analysis and reporting of clinical trial data. Specifically: creation of analysis files, tables, figures and listings (TFLs), validation of those files, and maintenance of associated tracking and validation documentation. Work is to be performed in a team environment, where team members may be distributed globally across several locations.
The Senior Programmer is expected to be able to provide technical and process-related guidance to team