Chloe Katz, Pmp Email & Phone Number

Worked cross-functionally to ensure clinical program processes are aligned, and that clinical activities adhere to research regulations and guidance, as well as organizational expectations. Served as the clinical trial operations representative for process creation, management, and improvement, as well as for monitoring implementation of processes. Worked.

I am so very excited and proud to be a part of this clinical team and company!

Chapel Hill, NC

Serve as Clinical Program Lead for observational, multi-center research studies.Develop research programs, including writing a protocol, plans, and stakeholder reports.Negotiate site budgets; ensure adherence to program budget. Conduct and oversee daily operations and strategic planning of all research phases. Facilitate team activities, including.

Durham, North Carolina

Led and oversaw the execution of monitoring services and daily site operations management for clinical trials according to the project-specific scope of work and budget, and Good Clinical Practices. Developed Clinical Monitoring Plans, Manuals of Procedures, Study Implementation Plans, templates, training documents and monitoring tools.Served as the.

Durham, NC

Manage contracts, overseeing financial planning and accountability, project timeline management and forecasting, contract & staff CRAsClinical monitoring.Manage research studies, including start-up and active-phase tasks, creating study manuals and ancillary research materialsCreate project templates and procedural manualsDevelop and manage SharePoint.

Create project templates and procedural manualsDevelop and manage SharePoint sites for study teams

Durham, NC

- Assisted Project Manager with study contracts and budget management- Managed subcontractors and vendor performance and payment- Wrote study-specific plans for implementation and presentation at sponsor meetings- Ensured continued IRB compliance- Managed central filing processes

Durham, NC

- In-house and on-site clinical monitoring of research protocols, including product accountability, regulatory file maintenance and study data review- Trained team members on study management processes

Durham, NC

- Audited site master files for completeness and accuracy

Chapel Hill, NC

- Provided coordination for data management and analysis for Public Health Leadership Development programs- Generated a codebook for reporting system indicators- Submitted IRB determination forms- Drafted a coding scheme for qualitative focus group data- Entered and coded data in Atlas.ti- Modified survey instruments- Interviewed project stakeholders.

Durham, NC

- Provided technical and regulatory assistance to clinical research project teams - Created and maintained tools to track site information- Prepared clinical trial materials for associates conducting site visits- Managed and audited project files and documents- Coordinated project start-up activities, including vendor communications, ordering supplies.

Durham, NC

- Provided technical and administrative support to clinical research teams conducting domestic and international trials. - Creating, maintaining and auditing a central files system for studies as they developed- Participating in and documenting weekly team meetings - Developing tracking tools and databases to monitor study progress and essential document.

Mali, West Africa

Water and Sanitation Volunteer- Designed and managed project funding for small-scale construction projects- Assisted administratively in the local health clinic- Delivered health education in a largely non-literate community using alternative education methods- Trained local populations and volunteers in water sanitation techniques

Mshs, Clinical Research Administration

Courses taken include research statistics, health policy and leadership, federal regulations and research ethics.

Mph, Public Health

Ba, French