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, In Form). • Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.). • Robust working knowledge of clinical trial terminology. • Must be able to work in a fast-paced environment. • Ability to work independently, take initiative and complete tasks to deadlines.
📌 Data Validator (Mumbai)
🏢 SIRO
📍 Mumbai