• Prepare and develop accurate source documents (eSource and paper) based on clinical trial protocols, ensuring compliance with GCP, 21 CFR Part 11, and internal SOPs. • Review and validate source documents to ensure completeness, accuracy, and alignment with study protocols, coordinating with site staff and internal teams for feedback and approval. • Maintain version control, track document updates, and implement protocol amendments efficiently while ensuring compliance with regulatory requirements. • Manage daily communication with site staff, study teams, and internal departments regarding source document updates, requests, and training support. • Organize, file, distribute, and archive source documents systematically for each clinical trial, ensuring proper documentation and accessibility. • Support quarterly initiatives, including process improvements, training development, and workflow optimizations for source documentation. • Participate in cross-functional meetings to provide input on study start-up timelines, protocol changes, and documentation impact analysis. • Conduct internal audits and quality checks to ensure adherence to documentation standards and regulatory compliance. • Develop and update standardized templates and checklists to improve the efficiency of source document creation.

• Treating patients via tele-health visits, including telephonic triage calls, video visit appointments, and email follow-ups • Continuous learning during weekly Clinical Rounds and through other modalities • Ongoing collaboration with both virtual and in-office teammates via daily huddles • Utilization of your specific clinical training and opportunities to give exceptional care to patients virtually

• Provide administrative support to the Grantmaking team. • Assist with program communications, updating the database, and organizing files and reports. • Graphic design and audiovisual content creation. • Create multimedia content for publication that uplifts the grant and fellowships projects. • Produce a variety of written pieces, which may include interviewing, audio transcriptions, translation, and short summaries on grant and fellowship projects. • Engage with different Indigenous communities and learn about the ongoing issues that affect them.

• Support enhanced vetting and polygraph operations for a U.S. government-funded law enforcement program • Conduct vetting and polygraph examinations on candidates in accordance with NCCA-accredited standards • Use simultaneous interpretation when the examinee does not speak English • Document examination results and prepare required reports • Maintain strict confidentiality and chain of custody for all examination materials and results • Coordinate with the Lead Polygraph Examiner and interpreters • Represent UG Solutions and the client in all interactions with host nation officials