Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.
- Knowledge of drug development process.
- Understanding regulatory requirements and relevant data standards; CDISC and SDTM knowledge and experience are preferable.
- Minimum 5 years’ experience in programming listings and/or visualizations with any of the following Veeva CDB, JReview and Elluminate.
- Hands-on experience with report development in Elluminate preferred.
- Experience with one of these languages: CQL, SQL, SAS, R, Python.
- Knowledge of clinical database systems (Metadata Rave, Veeva, InForm).
- Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).
- Strong working knowledge of clinical trial terminology.
- Must be able to work in a fast-paced setting.
- Ability to work independently, take initiative and complete tasks to deadlines.