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Job Description
Structured overview of role & requirementsAbout This Role
Develop and maintain clinical trial databases including electronic Case Report Forms (eCRFs) and edit checks using programming languages like C# and SAS.
Support programming of reports and listings for data review and analysis, ensuring standardization for external partners/vendors.
Contribute to development and maintenance of CDASH compliant therapeutic area and global eCRF libraries aligned with SDTM standards.
Minimum Requirements
Bachelor's degree in Computer Science, Mathematics, or related Science discipline.
Experience with Medidata Rave for building eCRFs, edit checks, and migrations.
Proficiency in C# programming for custom functions.
Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Familiarity with CDISC standards including CDASH and SDTM implementation guidelines.
Experience working collaboratively in a team environment with risk identification related to timelines and workloads.
Advantageous skills include SAS programming, Medrio, and Viedoc platform experience; MSc or higher in relevant field is a plus.