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I will review your clinical research protocol, consent, or irb package
Clinical Research Scientist and Consultant
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, methodolog...
About this Gig
Preparing a clinical research study, registry, observational study, or clinical trial?
I will review your protocol, informed consent form, recruitment materials, CRFs, and IRB submission documents and provide detailed feedback based on more than 20 years of clinical research experience.
I am a Clinical Research Program Administrator at Johns Hopkins University with extensive experience supporting investigator-initiated studies, industry-sponsored clinical trials, REDCap implementation, study startup, regulatory submissions, and research operations.
I can help identify:
- Missing or unclear procedures
- Inconsistencies between study documents
- Data collection gaps
- Workflow and feasibility concerns
- Recruitment and retention challenges
- Protocol and consent alignment issues
- Operational and regulatory considerations
- This service is intended to strengthen your study documents prior to submission or implementation.
Please contact me before ordering to discuss your project and determine the most appropriate package.
Database type:
Relational database
Platform:
MS SQL
•
MySQL
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PostgreSQL
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Other
Expertise:
Data structure
•
Design
•
SQL
•
Performance
Other Databases Services I Offer
FAQ
What types of studies do you review?
Clinical trials, observational studies, registries, survey studies, quality improvement projects, and other healthcare research initiatives.
Will you rewrite my protocol?
This service focuses on review and recommendations. Extensive document writing or editing may require a custom order.
Can you review informed consent forms?
Yes. Consent forms are one of the most common documents reviewed through this service.
Do you provide regulatory or legal advice?
No. I provide recommendations based on clinical research best practices and operational experience. Final decisions should be made by the investigator and their institution.
Can you review IRB submissions before submission?
Yes. I can review protocols, consent forms, recruitment materials, and supporting documents to identify potential issues before submission.
