• Assist project teams in compiling and synthesizing information (e.g., conducting literature reviews, policy scans, and Medicaid/TAF program research). • Prepare and assist with primary source data collection through interviews, focus groups, and surveys; organize materials; and contribute to content development. • Participate in the collection and review of research, evaluation data, and Medicaid/TAF program data. • Analyze quantitative and qualitative research data and contribute to the reporting and interpretation of findings. • Extract and transform Medicaid supplemental payment data into accessible formats (e.g., Excel/CSV) for quarterly reporting cycles. • Prepare documents, portions of reports, briefs, charts, and graphs that describe and interpret findings of analyses. • Support proposal writing and business development activities. • Support project management tasks, including developing project timelines, coordinating meetings, and tracking project progress.

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. • Collaborating with investigators and site staff to facilitate smooth study conduct. • Performing data review and resolution of queries to maintain high-quality clinical data. • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

• 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

• Support clinical trial site feasibility and site selection process • Conduct all aspects of clinical monitoring for clinical trials including conduct of site qualification visits, site initiation visits, routine monitoring visits and close-out visits at clinical trial sites • Support the maintenance of the Investigator Site Files and sponsor Trial Master Files • Conduct all aspects of site management as prescribed in the clinical trial specific functional plans • Prepare accurate and timely trip visit reports • Review progress of clinical trials, especially patient recruitment and clinical trial data capture, and initiates appropriate actions to achieve objectives • Organize and make presentations at Investigator Meetings • Participate in the development of Case Report Forms and clinical trial documents • Act as primary contact for clinical trial supplies and other suppliers (vendors) • Participate in regular clinical trial team meetings • Mentor less experienced or new CRA colleagues • Perform CTM tasks as appropriate and as delegated by the CTM • Proactively contributes to continuous improvement of Clinical Operation specific processes, procedure and templates