• Support the execution and management of clinical trials • Take responsibility for clinical trial monitoring deliverables • Assist in the planning, initiation, and execution of clinical trial activities • Conduct site feasibility assessments and participate in site selection processes • Coordinate with investigative sites to ensure compliance with study protocols and regulatory requirements • Monitor study progress and data collection activities to ensure quality and accuracy • Assist in the preparation and review of study documentation and reports

• Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s). • Ensures allocated tasks are performed on time, within budget and to a high-quality standard. • Proactively communicates any risks to project leads. • Provides system support (i.e., Activate & eTMF) and ensures system databases are always current. • Performs administrative tasks on assigned trials, including, but not limited to, timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, distributing mass mailings and communications as needed, providing documents and reports to internal team members. • May support scheduling of client and/or internal meetings. • May review and track of local regulatory documents. • Maintains vendor trackers. • Supports start-up team in Regulatory submissions. • Works directly with sites to obtain documents related to site selection. • Works in collaboration with teammates to achieve targeted goals for assigned projects. • Connect with the team and appropriate clinical personnel regarding site issues and risks.