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Joshua R
@joshrob0
Clinical Research Scientist and Consultant
Verenigde Staten
Engels
Over mij
I'm Josh, a clinical research scientist and consultant with 20+ years of experience across Phase I–III trials, device studies, and academic medical research. I help teams with study design, methodology, statistical analysis, data interpretation, manuscript prep, and publication support. I also advise on regulatory strategy, GCP compliance, IND submissions, and clinical operations.
My technical background in REDCap, EDC systems, and CRF design means I understand your data from protocol to publication—not just how to collect it, but how to analyze and report it.
Skills
Joshua R
offline •
Gemiddelde reactietijd: 5 uur
Bekijk mijn diensten
Database development
I will build, customize, or optimize your redcap project or research database
Ontwerp en optimalisatie
I will review your clinical research protocol, consent, or irb package
Werkervaring
Clinical Research Program Administrator
Johns Hopkins Medicine
Jun 2015 - Present • 11 yrs 1 mo
Lead operational, regulatory, and scientific oversight for ~10 concurrent clinical trials spanning rare disease, oncology, translational neuroscience, and imaging biomarker research. Serve as direct point of contact for industry-sponsored trials and site-level lead across multiple federally funded multi-site studies. Design REDCap/EDC systems, build CRFs, manage regulatory submissions, and support statistical analysis and manuscript preparation across an active research portfolio. Contributed to first-in-human and translational imaging research across Alzheimer's disease, Parkinson's disease, schizophrenia, and psychedelic neuroscience. Co-authored peer-reviewed publications with pharmaceutical industry partners on novel radiotracer and receptor-occupancy studies. Administered standardized neuropsychological/diagnostic assessments and supported protocol design for Schedule I compound studies.
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cps_nick
Terugkerende klant
Verenigde Staten
Josh is not only an expert in RedCAP, but he has a deep understanding of clinical trials. There were aspects within our CRFs that were a bit light in detail, and his recommendations rounded them out perfectly. He added intuitive logic, demo'd everything clearly, and was extremely professional throughout the entire process.
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