Skip to main content
IRB & IBC Resource Center
Client Logins & Support
Careers
Contact Us
Search for:
Search
Book a Consultation
Open Main Menu
Solutions
Solutions
Study Planning
Study Planning
Site Feasibility
Trial Design & Protocol Planning
Site Network for Sponsors and CROs
Quality & Compliance
IRB Review
IBC Review
Data Monitoring Committee (DMC)
Endpoint Adjudication Committee
Diversity, Equity & Inclusion
Statistical Consulting
Connexus
AIMS®
IRBNet
Your trial is what you make it.
Study Planning Overview
Study Review
Study Review
IRB Review
IBC Review
Endpoint Adjudication Committee
Data Monitoring Committee (DMC)
Statistical Consulting
Connexus
AIMS®
IRBNet
A single source of expertise for ethical and scientific review.
Study Review Overview
Site Enablement
Site Enablement
For Sites
Overview: Site Enablement for Sites
Study Start-Up
Coverage Analysis
Financial Management
Site Network
Site Resource Augmentation
Study Advertising
eResearch CTMS
For Sponsors & CROs
Overview: Site Enablement for Sponsors & CROs
Clinical Trial Training
Enrollment & Retention
InvestigatorSpace® Training & Safety Portal
End-to-end site optimization services to help you succeed.
Site Enablement Overview
Benchmarking, Analytics & Consulting
Benchmarking, Analytics & Consulting
Trial Design & Protocol Planning
Quality & Compliance
Diversity, Equity & Inclusion
Benchmarking & Performance Management
Statistical Consulting
Better data to guide better clinical operations decisions.
Benchmarking, Analytics & Consulting Overview
Enrollment & Retention
Enrollment & Retention
Participant Identification
Participant Recruitment & Retention
Study Advertising
My Patient®
Hit your critical trial milestones on time.
Enrollment & Retention Overview
Clinical Endpoints
Clinical Endpoints
Endpoints & Assessments
Cognitive Assessments
Rater Services
Remote Assessments
Imaging Core Lab Services
Endpoint Protection
Endpoint Adjudication Committee
Threat Detection
Statistical Consulting
eCOA/ePRO Platform
Study Insight Analytics
Confidently control your trial’s evidence data.
Clinical Endpoints Overview
Who We Serve
Who We Serve
Research Sponsors
Contract Research Organizations (CROs)
Research Sites
Research Participants
Solution Explorer
ClinSphere™
ClinSphere™
Explore The WCG ClinSphere™ Platform
AIMS®
Connexus
eCOA/ePRO Platform
InvestigatorSpace® Training & Safety Portal
IRBNet
My Patient®
Total Feasibility
Study Insight Analytics
eResearch CTMS
Clinical Trial Listing Service (CTLS)
Insights
Insights
Latest Insights
Patient Forum
Blog Posts
Videos
Whitepapers
Podcasts
Case Studies
Topics
Clinical Trial Operations
Diversity & Inclusion
Clinical Endpoints
Regulatory Compliance
Participant Recruitment
Site Efficiency
Clinical Trial Safety
In Focus
Clinical Trial Trends & Insights 2024
Blog Series: Ask the IRB & IBC Experts
Webinar Series: The Participant Playbook
Events
About
About
About WCG
Leadership
History
Careers
News
Policies
IRB & IBC Resource Center
Client Logins & Support
Careers
Contact Us
Search for:
Search
Book a Consultation
Brittani E. Nelson, MA, CLSSGB
Expedited Reviewer, WCG IRB
Latest insights by Brittani
Diversity & Inclusion
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
