Ergomed Enhances Clinical Trials Through Exceptional Investigator Support

By building strong relationships with investigators, we ensure their ongoing motivation to recruit the right participants and stay engaged throughout the trial. Our team helps engage principal investigators and site staff ahead of trial initiation by providing a forum for scientific discussion. Our study physician support team, located worldwide, has extensive experience in clinical practice and research and acts as a liaison between physicians. Understanding investigator and client needs is fundamental to a clinical trial’s success.

Our team provides direct support to investigators and patients in the following ways:

• Build Recruitment Plans
• Advise on Patient Eligibility
• Study-specific Site Training
• Swiftly Address Safety Questions and Concerns
• Sharing Best Practices
• Prevent Protocol Deviation Reoccurrence
• Represent the Sponsor
• Offer an Investigator’s Perspective

Our Study Physician Support team is composed of native speakers familiar with the local health system and has a broad network of local physicians. Ergomed’s specialized team of MDs supervises complicated or demanding trials and acts as a physician-to-physician liaison. Our clinicians improve training and compliance for local investigators, increasing recruitment rates and lowering dropout rates.

Our dedicated Site Management team works daily with investigators, study coordinators, nurses, and other site personnel. They support the site team in launching the study, helping prepare everything for patients, including all procedures and tests, and then engaging the team throughout the study. Our site managers are always available to provide advice and support — we never leave our sites unattended.

Ergomed Site Support Services enhance study site engagement through:

• Continuous Training
• Patient Recruitment
• Patient Retention
• Logistics and Administration

We deploy numerous strategies to relieve participating sites of some of the administrative burden of running a clinical trial, ensuring they have the time and resources they need to prioritize your trial and execute your protocol successfully. This includes site management customized to the unique setting of each study coordinator and execution mapping to ensure that every logistic and medical consideration and detail of the trial protocol has been carefully considered before the first patient visit.

This high level of site management support results in strong patient compliance, cleaner and better-quality data, faster enrollment, and higher patient retention. It also improves the patient experience and ensures that the approach at the study site is cohesive.