Role Description Make an impact while you learn. The Semester of Service Program offers students a volunteer project-based opportunity to support Federal missions, gaining hands-on experience & valuable career-ready skills. Students must be enrolled at least half-time in an accredited trade school, technical or vocational institute, junior college, college, university, or other accredited educational institution, & participation must be with the permission of the institution at which the student is enrolled. This vacancy announcement will be open from May 15, 2026 to May 21, 2026 or when 25 applications have been received. The vacancy will close on whichever day the first of these conditions are met. If the application limit is reached on the same day the announcement opened, the open and close date will be the same. Candidates are encouraged to read the entire announcement before submitting their application packages. Project Description: IO/PCA seeks a student assistant for a special project designed to increase the IO/PCA team’s understanding of Congressional Member and Committee sentiment towards the United Nations and other international organizations. This project has two main components: - Tracking Congressional hearings - Data input and analysis to an IO/PCA-maintained Member Biography database The student would be asked to: - Track relevant Congressional Committee websites for hearings with IO Bureau equities (i.e. on UN reform, fiscal responsibility, policies towards specific international organizations) - Watch the hearing and provide a readout to the IO Bureau - Collate a backlog of one year of Congressional Member statements and data input into an established database - Research public statements from Members (i.e. press releases, public hearings, interviews, proposed legislation) on the United Nations and other international organizations - Analyze the statements and input to an IO/PCA-maintained database to create a comprehensive biography of Members’ stances towards IO Bureau equities - Periodically update Committee rosters and membership, particularly if the semester falls over an election period Qualifications - Applicants will be considered based on their knowledge, skills or abilities related to project needs - Prefer student be currently enrolled in a bachelor's degree program - Students must have a minimum GPA of 2.0 out of 4.0 scale - Students studying abroad are ineligible for application - All remote work must be completed domestically within the United States Requirements - To qualify, you must be enrolled not less than half-time in an accredited trade school, technical or vocational institute, junior college, college, university, or other accredited educational institution - You also must be in good academic standing as defined by your institution - Attach a copy of your transcripts to your application package for verification

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

• Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

• Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. • Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. • Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting. • Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.