Marc Gregory Email & Phone Number

Greater St. Louis Area

* Lead the Planning and Setup, Monitoring, and Closeout phases of study management* Gather customer requirements and relaying to internal teams* Ensure the on-time development of the study documentation as defined in SOP or SWI, contributing and supporting as designated* Monitor budgets, initiate change orders and provide revenue forecasting* Provide risk mitigation and consultation for clients* Assist with software development and applications for clinical trials* Lead external and internal meetings* Act as a single point of contact for multi-service line projects* Prepare documents and databases for FDA and client-initiated audit inspections* Review medical images/reports for protocol adherence* Provide protocol training and support for international study centers* Assist with business development to secure new projects* Write and maintain trial documents* Maintain a working knowledge of current protocols

Greater St. Louis Area

* Assisted with the Planning and Set-up, Monitoring, and Closeout Phases of Study management* Coordinated Project meetings and assist with compiling meeting minutes and action items* Assistance with documentation/database updates due to scope changes* Follow-up related to invoice reconciliations* Preparation of reports in support of study forecasting activities* Facilitate issue Management by documenting and tracking progress to ensure timely resolution tocustomer escalations.

Greater St. Louis Area

* Maintained multiple clinical trial databases* Assisted site centers to ensure data is properly submitted to ensure timelines were met* Performed demographic QA of clinical trial data* Created and distributed data reports* Archived study data and documents