Clinical Project Coordinator
Current
Miami, Florida, United States
- Assist in production and formatting of study documentation e.g. informed consent forms, training materials, laboratory manuals, etc.
- Internal risk-based monitoring following first dosing to ensure all study documentation is working effectively.
- Assist with internal data generation such as recruitment and subject status, adverse event summaries, etc.
- Assist Project Managers with close out activities e.g. archiving, reconciliation.
- Manage data query resolution.
- General support to the Commercial and Project Management groups as needed to win and deliver business.