• Serves as a resource for NIH/NCATS policies, procedures, and use of eRA Commons HSS.• Identifies and implements process improvements and innovations.• Assists principal investigators and study teams to process manuscripts in accordance with the NIH Public Access Policy.• Participates in workforce development educational activities to principal investigators and study teams.• Collects mid-year and final progress reports from all awardees (e.g., pilots, trailblazers, KL2s) using… Show more • Serves as a resource for NIH/NCATS policies, procedures, and use of eRA Commons HSS.• Identifies and implements process improvements and innovations.• Assists principal investigators and study teams to process manuscripts in accordance with the NIH Public Access Policy.• Participates in workforce development educational activities to principal investigators and study teams.• Collects mid-year and final progress reports from all awardees (e.g., pilots, trailblazers, KL2s) using appropriate forms and required appendices.• Assists with the annual required RPPR compilation and submission to eRA Commons. Show less

• Served as the administrative resource and liaison in support of the business aspects of the clinical research enterprise. • Managed and performed activities related to multiple areas of clinical research administration including pre-award (budget development) and post-award (financial oversight) activities for multiple cost centers within Internal Medicine.• Ensured compliance with university policies, state and granting sponsoring agency. • Supported internal implementation of… Show more • Served as the administrative resource and liaison in support of the business aspects of the clinical research enterprise. • Managed and performed activities related to multiple areas of clinical research administration including pre-award (budget development) and post-award (financial oversight) activities for multiple cost centers within Internal Medicine.• Ensured compliance with university policies, state and granting sponsoring agency. • Supported internal implementation of general principles of GAAP standards in sustaining financial compliance and consistency with grant rules over the life of the project, following institutional and sponsor guidelines. • Performed a variety of technical and skilled duties involved in meticulously developing clinical research projects in accordance with established KUMC polices, federal, state, and industry regulations.• Utilized RedCap, Huron, Planner, Complion ebinder and the central unit inbox to support the day-to-day cross institutional management and compliance of clinical research.• Engaged in multi-dimensional responsibilities in nature, typically include various cross-functional duties and responsibility across multiple units of the organization. Show less

• Assisted in importing data collection/ data retention efforts such as transferring paper studies into the electronic system.• Provided training to the new IRB staff including Reliance Agreements, iMedRIS and Board meetings.

• Ensured that the Hospital’s clinical research activities are conducted in compliance with institutional SOPs and international, federal, state, and local rules and regulations and ethical principles regarding the use of human subjects in research. • Ensured that research activities at the Hospital involving human subjects are conducted in a manner that protects the safety, rights, and welfare of participants.•Assisted in assigning reviewers for full board and expedited… Show more • Ensured that the Hospital’s clinical research activities are conducted in compliance with institutional SOPs and international, federal, state, and local rules and regulations and ethical principles regarding the use of human subjects in research. • Ensured that research activities at the Hospital involving human subjects are conducted in a manner that protects the safety, rights, and welfare of participants.•Assisted in assigning reviewers for full board and expedited reviews.•Coordinated and attends IRB meetings including sending out review packets and monitoring meeting progress.•Writes meeting minutes post Board review for an accurate representation of meeting outcomes.•Reviewed research submission for completeness and proper content and communicate to investigators any deficiencies.•Acted as a liaison between reviewers and investigators to ensure any requested changes are made. Show less

•Provided customer support while resolving/escalating technical support problems for end users.•Resolved IT problems for faculty, staff and students via email, phone, or walk-up window.•Assisted with routine type hardware and software repairs.•Helped write technical documentation and assist with special events such as student orientations.•Assisted with the management of UMKC user accounts and permissions.

•Conducted research on poison prevention strategies.•Developed a quarterly calendar of social media content for both Twitter and Facebook to increase awareness of the Poison Helpline, Poison Center services, and poison prevention strategies. •Created support materials, such as charts, graphs, or other visuals to post online or to take to events.•Wrote internal communications for the poison control newsletter on the hospital's website.•Attended community meetings and conducted… Show more •Conducted research on poison prevention strategies.•Developed a quarterly calendar of social media content for both Twitter and Facebook to increase awareness of the Poison Helpline, Poison Center services, and poison prevention strategies. •Created support materials, such as charts, graphs, or other visuals to post online or to take to events.•Wrote internal communications for the poison control newsletter on the hospital's website.•Attended community meetings and conducted outreach to community stakeholders.•Represented the KUHPCC at community events.•Mailed out program materials as requested.•Data recording and entry. Show less