Clinical Trial Documentation Assistant
- Creating CRF modules and document templates for the affiliated SMO
- Compiling checklists from different sources to prepare more detailed versions


Enthusiastic Healthcare professional eager to contribute to team success through hard work, attention to detail and excellent organizational skills. Background in Healthcare field and well versed in: Clinical Trial Conduct & Monitoring, TMF IND/CTA, CRF design, IRB approval, CTSI & Site Selection/ Management IC, Subject Recruitment/Retention, Data collection/Data Management Query Resolution, AE/SAE reporting, ConMed Compliance, EDC/CTMS Audits, Labelling, Packaging, Shipping, Dispensing, Reporting, Archiving. Motivated to learn, grow and excel in Clinical Research Industry.