Study Design Specialist
Job Summary
Creating comprehensive study builds from start to finish in the CRIO platform, the part-time Study Design Specialist will develop eSource from protocols and eCRFs, conduct post-build quality control reviews, and manage complex trials remotely.
Key responsibilities:
- Utilize protocols, eCRF guidelines, and other source documents to produce comprehensive builds for clients
- Complete client-requested edits and customizations while ensuring timely completion of assignments
- Mentor and train current and new CRIO employees on the eSource module
Required qualifications:
- Experience with eSource and QC design in CRIO or other eSource/CTMS systems
- BS in a medical or sciences field
- At least 1 year of healthcare experience
- Ability to interpret clinical trial protocols and source documents
- Knowledge of medical terminology and procedures
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