• Project Management: Define project requirements, establish and track progress of study timelines and milestones against target dates. Ensure status, progress, and issues are communicated to stakeholders.• Leadership: Lead cross-functional team members to develop strategy and implementation plan for clinical trial through each phase of lifecycle. Effectively communicate goals and timelines so team members can effectively achieve project goals. Collaboratively problem solve through issues.• Clinical Data Management: Oversee data management activities for clinical research studies through the study lifecycle. Develop data management strategy, includes gathering data requirements and implementing efficient data management processes that meet regulatory standards in accordance with protocol and objectives.• Stakeholder Management: Act as primary point of contact and liaison for external stakeholders, fostering collaboration across diverse relationships in a dynamic environment.• Effective and Clear Communications: Lead, facilitate, and participate in internal and external meetings. Serve as subject matter expert, providing data management and operational guidance to site staff. Communicate complex or technical information in an organized and simple manner.• Develop, review, and maintain high-quality documentation: Draft, write, and review high-quality documents and implementation materials. Ensure documentation is complete and accurate, in compliance with SOPs and guidelines.• Training and Development: Develop training materials and train sites in data collection/data management processes, resulting in high data quality. Develop and present training materials for organization, related to internal processes.• Monitoring and Evaluation: Monitor/evaluate study data for compliance, completeness, and quality. Proactively identify issues through data analysis, develop and implement change control strategy, and provide written analysis report on findings and solutions.

• Recruitment and follow-up: Screened, recruited, and enrolled ~ 130 new participants per year and collected ~ 200 samples in total. Conducted and coordinated study visits efficiently and in accordance with study protocols, which included informed consent, questionnaire administration, and specimen collection.• Data Management, including data review, data collection, and data analysis: Conducted chart reviews to successfully screen and recruit eligible participants. Reviewed, collected data and prepared valuable datasets and reports to pharmaceutical collaborators. Gathered retrospective clinical data (composed draft abstract on chart review findings related to inflammatory arthritis), calculated clinical index scores, and prepared large datasets for internal scientists and external pharmaceutical collaborators. Improved and streamlined data collection efforts.• Project Management: Created project timelines and tracked milestones, including tracking and scheduling longitudinal study visits, drafting and submitting compliant IRB submissions, renewals, and modifications, and facilitated/completed scientist gatekeeper requests and collaborator requests. All deadlines were met and milestones completed on time.• Relationship Development: Cultivated excellent working relationships with physicians at Virginia Mason Medical Center’s main campus and satellite clinics to ensure successful recruitment of participants. Collaborated professionally with external pharmaceutical collaborators, provided strategic input into various projects, and maintained clear and effective communication. Developed rapport with participants through a positive attitude and calm confidence. • Operational Management and Training: Managed all operational issues related to the two translational registries. Trained new Clinical Research Coordinators/Assistants on study related functions, including protocol compliance, data collection, data entry, IRB submissions, and conducting study visits.