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$
USD
I will provide expert clinical research and redcap consultation
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
Planning a clinical research study, REDCap project, registry, or clinical trial?
I am a Clinical Research Program Administrator at Johns Hopkins University with 20+ years of experience supporting academic, government, and industry-sponsored research. I provide expert consultation on study design, REDCap implementation, CRF development, protocol planning, study startup, IRB submissions, clinical operations, and data management.
This consultation is ideal for investigators, physicians, researchers, coordinators, students, startups, and organizations seeking guidance before launching or modifying a research project.
Topics may include:
- REDCap database planning and workflow design
- Clinical trial and observational study design
- CRFs and data collection strategies
- Protocol development and feasibility review
- Study startup and operational planning
- IRB and regulatory considerations
- Recruitment and retention strategies
- Data quality and monitoring approaches
Please contact me before ordering to discuss your project and determine the best consultation package.
Database type:
Relational database
•
Other
Platform:
Other
Expertise:
Data structure
•
Design
•
ERD
•
Normalization
Other Databases Services I Offer
FAQ
What can we discuss during the consultation?
Protocol design, REDCap planning, CRFs, study workflows, IRB submissions, recruitment, data management, clinical operations, and study startup activities.
Do you build REDCap databases through this gig?
This gig focuses on consultation and planning. Database development services are available through my separate REDCap gigs.
Who is this service for?
Physicians, academic researchers, students, coordinators, biotech startups, nonprofits, and first-time investigators.
Can you review my protocol or consent form?
Yes. I can review protocols, consent forms, CRFs, schedules of assessments, and other study documents and provide recommendations.
Do I need prior research experience?
No. I work with both experienced research teams and individuals who are completely new to clinical research.
