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
WCG 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
Budget Development & Negotiation
Contract Review & Negotiation
CTMS Study Build and Support
Study Identification
Financial Management
Site Resource Augmentation
eResearch CTMS
For Sponsors & CROs
Overview: Site Enablement for Sponsors & CROs
Clinical Trial Training
Recruitment & 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
Recruitment & Retention
Recruitment & Retention
Identification
Enrollment
Retention
Documentation Support
Targeted Site Outreach
Study Advertising
My Patient®
A Simpler Approach To Your Study’s Recruitment and Retention
Recruitment & 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
Therapeutic Areas
Therapeutic Areas
Hematology/Oncology
Central Nervous System
Cardiovascular
Metabolic
Infectious Disease
Dermatology
Immunology
Gastroenterology
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
2024 Clinical Research Site Challenges Report
Blog Series: Ask the IRB & IBC Experts
FDA Guidance Portal
Events
About
About
About WCG
Leadership
History
Careers
News
Policies
Certifications
IRB & IBC Resource Center
Client Logins & Support
Careers
Contact Us
Search for:
Search
Book a Consultation
Bridget Brave
Director, Expedited Review IRB Operations
Latest insights by Bridget
Ethics in Clinical Research
Review of Emergency Research
Whitepapers
Ethics in Clinical Research
What Is Exempt Research?
Blog Posts
Ethics in Clinical Research
What Is Expedited Review?
Blog Posts
