Orange County Metro Area, CA
- Responsible for efficient processing and quality check of all study documents
- Review and ensure accuracy and completeness of clinical study files
- Organize documents and data in ETMF (electronic trial master file), CTMS (clinical trial management system) and ensure compliance with internal procedures.
- Collate new study materials, create study binders, patient recruitment materials, and arrange shipment of materials to clinical sites
- BS in life sciences or related field with 1-2 years of experience
- Experienced with Clinical Systems including CTMS (Clinical Trial Management System) and eTMF (electronic Trial Master file) preferred
- Ability to manage competing priorities in a fast paced environment