JOB RESPONSIBILITIES :
- Support and / or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones.
- Integration of data across studies in support of CSS / CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.
- Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).
- Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.
- Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.
- Participate in department working groups; provide input in development of tools and improvement of processes.
JOB REQUIREMENTS : Education
Masters DegreeAlso acceptable - MS. in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.SAS Certification desirable.EXPERIENCE :
3 – 5 Year