- Assessed drug storage conditions and procedures to check adherence to standard protocols
- Achieved project objectives by working closely with teammates
- Developed extensive database to organize specimen collection, processing, storage, and created efficient centralized records system
- Reviewed the site regulatory binder to check collection procedures and completeness of paperwork
- Adhered to good clinical practices, operating procedures and regulatory requirements
- Managed blood specimens for clinical trials and processed specimens for sample storage and assay
- Participated in educational training, activities, and professional development programs.