Back
Niche clinical CDISC/Medidata skills lower applicant density despite remote role broadening reach.
Clinical trials standards (CDISC/SDTM) and eCRF tools make skills highly industry-specific and less transferable.
Mandatory CDISC, Medidata Rave and C# skills create moderate rigidity without explicit years requirement.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
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.
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.
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.