• Develop a strategic and comprehensive privacy program in alignment with regulatory standards • Establish and enforce policies ensuring the confidentiality of protected health information (PHI) • Manage privacy-related committees and initiatives in coordination with the Vice President and General Counsel and Director of Audit • Provide leadership in training and educating the workforce on privacy matters • Collaborate with IT Security and Information Services to integrate privacy and security programs • Develop and maintain metrics and reports to assess privacy compliance and risk analysis • Monitor compliance activities and assess privacy concerns in coordination with other compliance functions • Oversee compliance of business associates and business associate agreements related to privacy • Manage the process for receiving, investigating, and addressing privacy-related complaints • Ensure timely compliance with breach notifications as per HIPAA and state laws • Conduct information privacy awareness activities and provide training to Baylor Genetics teams • Work on litigation and administrative matters related to privacy issues in coordination with legal counsel • Supervise the Regulatory and Compliance Manager, assigning duties as necessary • Develop strategies to ensure compliance with various regulations like GDPR, FERPA, PCI, among others

• Independently work with clients to prepare compliance documentation, including export, FCC, and NOAA license applications, classification analyses, technology control plans, registration statements, annual and semi-annual reports, and other compliance program documentation. • Train and oversee the work of case assistants on export controls and FCC licensing. • Track regulatory developments, support engagement with regulators, prepare and edit internal guidance, create client alerts, and other substantive non-billable materials. • Support business development efforts through development of pitch materials, attendance at aerospace and defense industry-focused conferences, and development of client alerts related to national security, trade topics and other regulatory matters. • Support other team projects on an as needed basis. • Maintain compliance with all firm policies and procedures.

• Liaise with SAR colleagues to drive plan, organize, compile, progress, track, and submit regulatory submissions on a timely basis and with a consistently high level of quality. • May act as a contact point for translation review of submission documents such as applications, synopses, ICFs, labels, etc. • Maintain country-specific patient information sheet and consent form customization text. • Maintain country-specific drug labeling information and Country Intelligence Pages. • Review and make recommendations on all relevant documentation e.g. labels, patient information sheets, diary cards etc. to comply with ICH GCP & country-specific requirements.

• Ensures compliance with federal and state laws, regulations, and rules governing healthcare entities • Identifies risk areas, prepares audit tools, conducts audits, and provides analysis and recommendations to executive leadership • Conducts audits and provides support for other internal or external auditors • Investigates and resolves compliance issues related to the healthcare environment • Evaluates regulatory agency reports and formulates responses and corrective actions • Maintains logs, indexes, files, computer databases, and other records pertaining to compliance and risk • Creates logs and systems for entering and tracking compliance guidelines • Confers with administrative staff regarding compliance risk areas and final reports • Develops strategies and leads compliance related committees/work groups • Implements compliance procedures • Responsible for ensuring compliance with governmental requirements