I will provide expert clinical research and redcap consultation
Clinical Research Scientist and Consultant
Nivel 1
Ha cumplido determinados criterios de rendimiento y muestra un gran potencial en la plataforma.
Acerca de este Servicio
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.
Tipo de base de datos:
Base de datos relacional
•
Otros
Plataforma:
Otros
Experiencia:
Estructura de datos
•
Diseño
•
erd
•
Normalización
Otros servicios de Bases de datos que ofrezco
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.
1 comentarios sobre este Servicio
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Desglose de calificaciones
- Nivel de comunicación del Freelancer
- Calidad de la entrega
- Valor de la entrega
Ordenar por
C carmenbaezfra

Puerto Rico
Excellent experience!!
USD 800-USD 1,000
$
7 días
Tiempo
Útil?
1 comentarios sobre este Servicio
| (1) | ||
| (0) | ||
| (0) | ||
| (0) | ||
| (0) |
Desglose de calificaciones
- Nivel de comunicación del Freelancer
- Calidad de la entrega
- Valor de la entrega
Ordenar por
C carmenbaezfra

Puerto Rico
Excellent experience!!
USD 800-USD 1,000
$
7 días
Tiempo
Útil?
