Foster strong partnerships with faculty, driving innovation in clinical trials and ensuring seamless execution of research initiatives.Oversee the drafting and editing of clinical trial protocols, refine consent development, and CRF design processes to enhance data accuracy, bolster participant safety, and ensure scientific rigor and compliance.Create and validate 29 CFR Part 11-compliant study databases and EDCs, ensuring adherence to regulatory standards and improving data management processes.Develop search criteria for grant opportunities and RFPs in relevant areas, and liaise with foundations to identify and secure project support.Develop grant-related content, including proposals, letters of intent (LOIs), executive summaries, and descriptions of facilities and resources.

Spearheaded comprehensive research administration in non-oncology space across an 11-hospital system, enhancing pre- and post-award processes and leading strategic healthcare innovation initiatives.Directed Research Compliance, ensuring regulatory adherence by managing disclosures, implementing educational programs, resolving conflicts of interest, and conducting monitoring activities. Developed and implemented a new tracking system to enhance the management of disclosures and management plans, significantly improving efficiency and oversight.Orchestrated cross-functional teams to align research objectives with organizational goals, driving strategic growth in healthcare innovation.

Managed research billing, ensuring financial integrity and compliance in invoicing and payment auditing.Led grants team, optimizing budget management and fund allocation, achieving precise expenditure reconciliation.Developed policies for compliant research practices, maintaining solid record-keeping.Orchestrated Award Review Board operations, evaluating grant applications for compliance and feasibility.

Managed a diverse team to ensure the smooth execution of Principal Investigator (PI) initiated studies, enhancing team productivity and project efficiency.Led new study initiatives, including RWE projects, from concept through to execution, ensuring timely delivery and adherence to project milestones.Developed and implemented procedures for Good Clinical Practice (GCP) compliance, including training staff on essential protocols to ensure patient safety.

Division of Parasitic Diseases and Malaria/Center for Global Health (CGH/DPDM)