Skip to main content

IRB & IBC Resource Center
Client Logins & Support
Careers
Contact Us

Search for:

Book a Consultation

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

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

For Sites
For Sponsors & CROs

End-to-end site optimization services to help you succeed.

Site Enablement Overview

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

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

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

Research Sponsors
Contract Research Organizations (CROs)
Research Sites
Research Participants

Hematology/Oncology
Central Nervous System
Cardiovascular
Metabolic
Infectious Disease
Dermatology
Immunology
Gastroenterology

Solution Explorer

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)

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 WCG
Leadership
History
Careers
News
Policies
Certifications

IRB & IBC Resource Center
Client Logins & Support
Careers
Contact Us

Search for:

Book a Consultation

Videos
Ethics in Clinical Research

Do the Right Thing: Unique Ethical Issues in Oncology Research

Share

Lindsay McNair, MD, MPH, MSB

Chief Medical Officer, WCG (Former)

Download Report

Ask the Experts

Our experts answer your clinical trial questions, and share the (anonymized) answers as a resource for our industry.

Ask a question now

More Ethics in Clinical Research

See All

Ethics in Clinical Research

Honoring Childhood Cancer Awareness Month: The Legacy of Innovative Treatments

Ethics in Clinical Research

What Is the Role of a Legally Authorized Representative in Informed Consent?

Ethics in Clinical Research

Demystifying FDA Processes: Why Do Changes in Regulations Take so Long?

MAGI 2025

May 18, 2025 - May 21, 2025 @ Boston, MA

General Inquiries

609.945.0101
[email protected]

Office Locations

Client Logins & Support

IRB Support

855.818.2289
[email protected]

Book A Consultation

Solutions

Study Planning
Study Review
Site Enablement
Recruitment & Retention
Benchmarking, Analytics & Consulting
Clinical Endpoints

About

Careers
About WCG
Leadership
News

Insights
Events

Get to the latest in news & insights

Solutions
Events
About WCG

Get to the latest in news & insights

Client Logins:

WCG IRB Connexus
InvestigatorSpace
Virgil
Latitude
My-Patient.com

Copyright 2024 WCG Clinical. All rights reserved.

Privacy Policy
Terms of Use
Do Not Sell Or Share My Data
Site Map