Clinical Project Coordinator
Current• 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.