amy scott

Multifaceted, evolving, and efficiently disseminating and integrating changes. Perform all duties from previous position in Cancer Research.

Applying accounts receivables, line item identification of funds, setting-up accounts with automated payroll integration, participating in external audits documentation needs, and experiencing record retention moving from paper to electronic format has been a valuable asset to incorporating didactic to application. My teams of coworkers are in silos of tasks; however, we interact in driving quality products in accordance with guidelines and regulations.

Primary function of 2014 has been in navigating and facilitating training to Researchers within IRBNet data management system for IRB Human Subject Research. During the data conversion "pre"-registered Researchers with existing protocols and facilitated one-on-one, group, or self-paced training material. Developed self-paced written tutorials, power point presentations and information sheets: office procedures, board members, and researchers. Coordinated a Community Research Collaboration Meeting targeting local research entities. Developed training material, resources and created booklets for the networking which highlighted the requirements for protocol submissions to the Internal Review Board (IRB).

Developed and implemented sustainable evidence-based activities to engage participants with cognitive or age related health disabilities using structured yet enjoyable exercise activities to promote stretching and range of motion. Analyzed current practices and then created a student orientation guide to help facilitate understanding of the adult health needs; including an overview of reportable incidents to aid in avoiding harm to clients and students and incidents of liability.

* Work independently and with cancer research team to provide effective and efficient monitoring of biomedical research at hospital site. * Coordinate regulatory requirements. * Ensure federal, state, and protocol specific documentation is completed by physicians and staff. * Compile site level IRB submission. * Collaborate with sponsor monitors. * Provide timely response to all inquires. * Resolve compliance issue independently and with team.

As a research analyst I navigate between revenue recovery, administrative, clinical trial regulatory, and the intersection of each role to maintain company, contractual, state, and federal compliance. My broader role allows me to apply my education in practical activities to have a meaningful impact not only for the business end but for patients in our Northern Nevada community who seek to participate in cutting edge clinical trials for both the potential self-benefit and the generalizations from data collection during their enrollment in the study. I am a human asset for Renown Regional Medical Center. The value I add to the health system is a bridge from frontline patients/participants, navigating systematic documentation for quality and life safety, and ultimately a return on investment for offering clinical trials at Renown Health.