• Execute clinical monitoring activities at clinical trial sites • Monitor clinical trials in accordance with ICH guidelines and GCP • Collaborate with Regional Clinical Operations Manager to ensure study timelines are adhered to • Identify gaps and propose CAPA • Conduct monitoring visits and complete visit reports per standards • Manage sites and site performance regarding regulatory submissions

• Research, analyze, and evaluate current year state tax forms, vendor specifications, letters of intent, and requirements to identify, document, and advise company of tax changes impacting company compliance with state Departments of Revenue (DOR) • Assist tax software developers by researching and answering tax related questions • Use developed research skills to unravel moderately complex tax situations into the fundamental tax points as they are applicable to current, proposed, or past law • Make recommendations to tax product teams on forms that may need to be added to or removed from the existing suite of forms • Coordinate, develop, and/or assist in researching tax issues to support other corporate departments such as Government Relations, Media Relations, Marketing, Legal, Insurance, Software Development, Pricing & Analytics, and Field Training • Coordinate and/or participate in work teams as necessary for the analysis and preparation of summaries of passed and proposed tax law • Edit, review, and fact check a variety of tax-related materials produced by self and others to verify accuracy and completeness of material • Ensure that assigned projects are completed on or before agreed upon deadlines

• Review database search results (SSN Trace, Nationwide Criminal Database) to determine additional names or searches needed. • Perform criminal record research through various court access systems and public records. Contact courts and verified sources via phone, email, fax, and mail when additional research is required. • Apply company guidelines, federal and jurisdiction-level regulations, and client-specific rules when processing requests. Document all actions taken within internal and client-facing notes. • Compile accurate, compliant consumer reports for Foley clients. • Communicate internally with quality control and other team members to ensure timely, high-quality results. • Communicate externally with customers and vendors as support needs arise. • Contribute ideas to improve processes and collaborate across departments. • Work across numerous platforms, while implementing new tools and strategies to drive the business forward for our customers

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures, GCP and ICH guidelines, and applicable regulatory requirements. • Perform all required monitoring activities to ensure subject safety, data integrity, and quality. • Verify the protection of study participants through informed consent procedures and protocol compliance in accordance with regulatory requirements. • Review CRFs (electronic or paper) and subject source documentation for validity, completeness, and accuracy and verify proper management and accountability of Investigational Product. • Prepare timely monitoring visit reports, document findings and corrective actions, update required tracking systems, and escalate issues as appropriate. • Ensure Investigator Site Files (ISF), eTMF documentation, CTMS records, and other study documentation are maintained in accordance with GCP, ICH guidelines, and regulatory requirements. • Support project-related activities including review of monitoring reports, site assessment visits, audit and inspection readiness, mentoring of CRAs, and other activities as required.