Udy Okaro

Provide scientific expertise throughout the development, execution, and reporting of clinical studies. Develop clinical trial protocols, protocol amendments, clinical study project timelines, and scientific publications using knowledge of implanted medical device therapies. Interacts with cross-functional teams to assist in the development of clinical strategy, study plans, reports, and deliverables.

Critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor, and absence of bias Developed and authored the RECOVER COVID Adult protocol Maintain timelines and workflow of writing assignments such as MOP, Informed consent, IRB protocol. Highly proficient with styles of writing for various regulatory documents Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary

Plan and execute biological research. Conducts and leads multiple research project. Review, interpret and report data. Author scientific publications. Train military personnel on microbial techniques like microbial isolation. Track, update and implement project changes. Review, interpret and communicate clinical data from all phases clearly as reports, presentation or applications to facilitate efficient submission and approval. Provide scientific and administrative support for clinical projects. Knowledge of drug development process.

Developed and validated protocols. Conceptualized biomedical research. Authored 5 scientific publications and 2 successfully funded grants. Work with internal review personnel to ensure successful grant application. Multiple public speaking engagement to both scientific and non-scientific audience. Interpreted lab data succinctly. Review data output for accuracy and consistency.

Collecting, maintaining, and reviewing documents necessary to ensure regulatory compliance. Collaborated with CROs to maintain project timeline.

Reviewed, analyzed and interpreted patient clinical trial data for CER reports. Maintained clinical coordinators training records. Tracks and maintains project content for post market surveillance (prescribing information). Access relevance of published literature and patents to vaccine.

Allergy and Infectious Diseases concentration. Studied the control of a major adhesin required for biofilm formation and virulence in Bartonella henselae.