• Join as a Clinical Trial Coordinator and provide administrative and technical support to the Project Team. • Support audit readiness by ensuring files are reviewed according to the schedule. • Provide administrative support for site activation activities. • Develop collaborative relationships with investigators and site personnel. • Analyze and reconcile study metrics and findings reports. • Maintain vendor trackers and assist with study-specific materials.

• Provide administrative and technical support to the Project Team • Assist with audit readiness and site activation activities • Develop collaborative relationships with investigators and site personnel

• Coordinates, oversees and completes functions on assigned trial(s) activities • 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 and ensures system databases are current • Performs administrative tasks on assigned trials • Analyzes and reconciles study metrics and findings reports • Supports start-up team in regulatory submissions • Collaborates with teammates to achieve targeted deadlines

• Coordinate, oversee and complete functions on assigned trials activities detailed on the task matrix • Perform department, Internal, Country and Investigator file reviews as assigned and document findings in appropriate system • Ensure allocated tasks are performed on time, within budget and to a high quality standard • Proactively communicate any risks to project leads and line manager as appropriate • Support the maintenance of study specific documentation and global support with specific systems, tools and trackers • Provide system support (i.e. GoBalto & eTMF) • Support RBM activities • Perform administrative tasks on assigned trials including timely processing of documents sent to Client (e)TMF as assigned • Support scheduling and organization of client and/or internal meetings with completion of related meeting minutes • Review and track local regulatory documents • Transmit documents to client and centralized IRB/IEC • Analyze and reconcile study metrics and findings reports