• Support the project team lead by assisting in the development and execution of project plans, including tracking deliverables, milestones, and outcomes. • Develop clear and compelling policy briefs, reports, presentations, and communication materials that translate complex research, policy analysis, and project conclusions into actionable insights and recommendations for diverse audiences. • Support the design and execution of research to improve student success. • Collaborate closely with senior team members to conduct qualitative and quantitative research, including supporting data collection activities (e.g., interviews, focus groups, case studies), conducting data analysis using publicly available data, conducting secondary research and synthesizing findings from higher education research and policy. • Build and sustain strong relationships with FoundationCCC partners, the Chancellor’s Office, and other higher education, government, and nonprofit partners. • Stay attuned to federal, state and system office policy development efforts by attending Chancellor’s Office events, Board of Governors meetings, legislative hearings and briefings, and other relevant meetings, virtually or in-person.

• APEX Clinical Research Associate (CRA) providing foundational clinical research training • Perform billable project tasks to support CRAs and Clinical Operations Leads • Collaborate with CRAs for observational and co-monitoring support • Address and resolve site issues and questions • Manage site quality and delivery from site identification through to close-out

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol • Communication with the medical site staff including coordinators, clinical research physicians and their site staff • Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff • Medical record and research source documentation verification against case report form data • Ensuring good documentation practices are adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements • Verification that the investigator is enrolling only eligible subjects • Regulatory document review • Medical device and/or investigational product/drug accountability and inventory • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol • Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement • Completion of monitoring reports and follow-up letters, summarizing significant findings, deviations, deficiencies, and recommended actions to secure compliance

• As a freelance contributor, you will work on a project basis, delivering high-quality analytical insights across several areas, including: Company Profiling: Analysing businesses by collecting and processing financials, and synthesising business, market, and M&A track record overviews • Deal Opportunity Mapping: Forming integrated views on platform and add-on deal opportunities for leading PE clients, supported by our proprietary technology • Sector Research: Contributing to research initiatives and niche sector analyses regularly • Platform Insights: Providing feedback and support for ad-hoc projects aimed at enhancing platform data and project efficiency