Scientific Leadership Team

From leading drug development experts to principal investigators and operational managers, ERG has assembled a team of industry leaders whose expertise spans multiple therapeutic areas and over 50 specific indications across all stages and types of clinical trials. We offer their knowledge to sponsors and clinical research organizations, helping identify opportunities and avoid potential pitfalls as you plan and implement your clinical trial.

Protocol Design and Review

A strong protocol sets the foundation for ensuring patient safety, collecting high-quality data efficiently, reporting results promptly, and supporting future regulatory requirements. ERG harnesses deep knowledge of specific therapeutic areas to help you design the optimal protocol for your clinical trial. Indeed, our rigorous review process includes staff from any discipline that will “touch” that protocol, from principal investigators and clinical operations staff to regulatory, recruitment, pharmacy, and quality assurance personnel. This service is provided at no cost as a professional courtesy. We can also connect you to professional medical writers—often from among our advisors—who we can recommend as paid resources to write your protocols.

Vendor Resourcing

Vendor selection can be daunting. ERG can help. Having worked with most established clinical research vendors, we bring hands-on knowledge. We are happy to recommend vendors based on your specific program needs—including many of our own consultants—or to simply offer insights into vendors you are considering.