Angel Sherrill Email & Phone Number

Greater Nashville Area

• Manages relationships and operations between vendors, study sponsors, and sites to promote high operational standards and protocol compliance for 3 multi-site trials.
• Assists in the facilitation of internal collaboration between cross-functional teams (Safety, Medical Monitoring, Regulatory, Data Management, Program Management, Medical Writing, Biostatistics, and Statistical.
• Proactively tracks data, accrual, site activation, and other important targets while implementing plans to make improvements where needed.
• Creates and maintains study specific clinical operations documents, plans (Clinical Monitoring Plan, Recruitment Plan, Communication Plan, etc.) and tools for managing study team performance metrics. Multiple clinical.
• Collaborates with CRA Line Managers to resource, train, and manage 3-4 Clinical Research Associates (CRAs) per assigned trial in compliance with the trial’s Clinical Monitoring Plan and within budget.
• Utilizes functional knowledge and site feedback during protocol reviews to provide operational feedback that was adopted in multiple study protocols.

Greater Nashville Area, TN

• Facilitated the execution of 9 phase II-III clinical trials by coordinating the efforts of clinic, regulatory, laboratory, and the clinical support teams
• Provided oversight for screening, enrollment, CRF completion, and study logistics while ensuring compliance to HIPAA, Human Subjects Protection, Good Clinical Practice Principles, and other applicable guidelines
• Reported adverse events, serious adverse events, protocol waivers, deviations and violations to both sponsor and Regulatory Affairs as outlined by the study guidelines set by the IRB
• Acted as liaison between SCRI Clinical Operations and sponsoring companies / clinical research organizations
• Created tools to efficiently track clinical, financial, and administrative information during all stages of assigned clinical trials
• Created protocol-specific tools that reduced unplanned deviations related to patient visit scheduling

Greater Nashville Area, TN

• Ensured the smooth and efficient day-to-day operation of research and data collection activities for a multi-million dollar research study
• Coordinated and assisted in the facilitation of participant recruitment community outreach, emails, and other marketing efforts
• Acted as the primary administrative point of contact for internal research staff, oncologists, and for other organizations
• Created Standard Operating Procedures to ensure adherence to protocol specified research standards.
• Facilitated the Institutional Review Board approval process to ensure study compliance to University, State, and Federal guidelines
• Conducted both qualitative and quantitative data collection (i.e. focus groups, cognitive interviews, and distribution of surveys)

• Assisted with health outreach programs (e.g. cancer prevention, health education, tobacco cessation, childhood obesity prevention, and other projects to reduce health inequities)
• Worked to support the Vanderbilt-Meharry-Tennessee State University cancer alliance in various multi-site studies and cancer outreach initiatives.
• Designed quantitative and qualitative instruments
• Quantitative and qualitative data collection
• Conducted participant interviews and surveys
• Performed health-related research (with a particular emphasis on chronic disease, health inequity and medically underserved populations)

Mph, Public Health

Concentration: Cultural Competency

B.A., Psychology

Activities and Societies: Phi Beta Kappa Honor Society, W.E.B DuBois University Honor Program, Psi Chi Psychology Honor Society, RAGE Fisk.

High School Diploma, Honors