Experience: 2 to 4 years in the pharma industry, with at least 2 years setting up clinical trial databases (such as Veeva EDC or InForm).
Technical Skills:
Experience with Python, SQL, R, or SAS.
Hands-on experience with Azure Databricks. Roles and Responsibilities:Responsible for design and set-up of study database (EDC and CDMS build) leading upto SDTM data
generation, for data collection in clinical trials, with medium to high complexity.
 Responsible for data ingestion and establish the data flow, achieve single source of truth and stand-
ardization for end consumers in the value chain.
 Facilitate Clinical data acquisition, data processing, transformation and harmonization of external Data as
per trial/project needs.
 Ensure testing is performed and database meets specification requirements before deployment into
production.
 Create and maintain system related documentation.
 Supporting suppliers and internal stakeholders using Managed File Transfer Process and CDMS load
status responsibilities.

experience

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