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.).

• Solid 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