Meghan Hosely

A clinical trial management system (CTMS) can bring powerful efficiencies, insights, and compliance to sites' day-to-day operations.

Rosamund Round VP of Parexel’s Patient Innovation Center and DCTs shares key strategies for increasing diversity in decentralized trials.

eConsent is a way to enhance the patient experience through improved study design, retention rates, and communication.

Aside from being a regulatory and ethical requirement, informed consent is a good way to ensure participant knowledge and develop a foundation trust between researcher and participant.

Learn how to write effective edit checks in electronic case report forms (eCRFs) to help improve data quality in electronic data capture systems.

Clinical Research Coordinators are tasked with many responsibilities throughout the day. Learn about balancing each role and responsibility effectively.

Gain a better understanding of clinical trial budget negotiations to reduce delays and study startup times.

Learn more about coverage analysis, the process to determine if an item or service is part of a patient's standard of care or covered by Medicare.

The COVID-19 pandemic forced organizations to adjust to continue high-quality research, positioning research to be more patient centric and streamlined.

Advarra offers a number of services to help you restart your short- or long-term research activities, such as Staff Augmentation.

The site-sponsor relationship is multi-faceted. The need for communication and understanding between the two is prevalent now more than ever.