Description
- Provides consistency and quality assurance across various projects.- Collaborates with Biostatisticians or Clinical Data Managers in defining macro specifications.
- Demonstrates significant contribution to the improvement of global macros.
- Provide support for Application Development, Clinical Programming, Biostatistics requests.
- Assist in the preparation of submissions of electronic data (e.g., SAS® data sets) to regulatory agencies.
- Contributes to strategic initiatives.
- Experience in Statistical programing and Clinical programming strongly favorable.
- Knowledge of database programming, Linux Operating system, and CDISC, eCTD a plus.
- 6 years of experience and a BS degree in Biostatistics, Computer Science or equivalent.
- 2 years of experience and a MS degree in Biostatistics,/Computer Science or equivalent.
- 1 year of experience and a PhD degree in Biostatistics/Computer Sciences or equivalent