• Writing about scientific research and new technologies
• Joining R&D clients to discus projects and initiatives being developed at some of the largest companies in the United States
• Taking notes to capture an understanding of the background of the product or process, the technical challenges faced by the client's R&D team, as well as the process of experimentation to try to resolve those technical challenges
• Drafting narratives or filling out standard questionnaires that relay the "stories" of these research & development efforts in order to support R&D Tax Credit claims

• Provided program support and documentation for NC FAST, enabling local families to access essential resources
• Created content for county representatives and internal teams, including instructional guides, technology support, metrics/reports, and funding presentations
• Provided cohesive project management outlines among various stakeholder for a facility move

• Supported expedited licensing submissions of gene therapy products to the FDA/CBER
• Composed tracking matrices from SAP and audited them with numerous sources such as Certificates and shipping records, to ensure reliability, accountability, and accuracy.
• Performed data verification of technical documents, such as specifications, protocols, reports, master batch records (MBRs), and master formulation records (MFRs)
Professional Experience (continued)

• Interfaced with physicians to bridge clinical needs
• Provided creative solutions through written copy for design assets
• Built and refined clinical training tools, engagement experiences, and customized knowledge exchanges from conceptualization to implementation
• Interpreted clinical and regulatory documents to ensure the creation of accurate tools
• Incorporated instructional design, adult learning principles, and behavioral sciences
• Integrated feedback from SMEs, medical and behavioral scientists, training architects, content designers, and proofreaders/formatters

• Edited and compiled surgical device reports for EU MDR regulatory approval
• Wrote design verification reports with statistical analysis for surgical device

• Edited multiplatform training materials, and compiled reports showing adherence to protocols
• Provided training subtitles for accessibility

• Provided comprehensive editing of board certification exam and promotional materials
• Led live-editing conferences with pediatricians and test developers to create content
• Ensured consistency of materials and quality of user experience across platforms
• Responsible for project management of four subspecialties

• Wrote and edited study reports, proposals, publications, and online user guides
• Authored in-house style guide and created report templates
• Ensured compliance with regulatory guidelines
• Assisted with statistical evaluation, data curation, and quality control
• Provided plain language review for 508 compliance

• Prepared assay plates from chemical samples via compound handling procedures
• Served as point of contact for resolving chemical-submission issues with scientists
• Co-authored a risk assessment
• Created and presented a problem-solving automation procedure
Professional Experience (continued)

• Collaborated with stakeholders to coordinate departmental training requirements
• Created original process flowcharts for document control processes
• Maintained compliant QA documents and training records across platforms
• Supported a successful internal audit