Clinical Trial Management

As your clinical trial and site management partner, we go to great lengths to support your sites and their patients.

We provide a variety of tools and support mechanisms to prepare for trial success. Our Clinical Trial Manager is responsible for ensuring sites are set up for success and fostering a relationship which starts at site feasibility and builds through activation, maintenance, and closure. The ultimate mission of our clinical team is to ensure the rights, safety, and wellbeing of trial participants, while focusing on data and scientific integrity.

Our philosophy is straightforward: our site management and monitoring team helps site staff overcome study challenges by building deep and enduring relationships. We recruit team members who are empathetic, great listeners and communicators, because building trust between the site staff and the Emmes project team is paramount.

We're different because we bring a collaborative approach to site management. We become site and patient advocates starting with protocol development by providing input to ensure protocols are operationalizable and minimize burden on site staff and patients.

Our data managers are both integrated study team members and therapeutically aligned, so they understand the context behind the data. Clients and sites benefit from system training sessions, frequent interactions and the opportunity to ask questions.

From study planning and protocol development, and paying attention to the operational feasibility, we ask all the right questions: Can sites comply logistically with the protocol? Is the visit schedule and testing regime too burdensome on patients? How easy will it be to collect, enter, and manage the data? What support will sites require to manage protocol and regulatory compliance issues?

By approaching the protocol design from various perspectives, we can work with you to create an operationally sound and appealing trial.

From study launch, our clinical study team and data management professionals work closely to ensure correct and timely data entry. We review your patients' laboratory results to make sure the values are within range and patients remain safe during the trial. We collaborate with sponsors and internal clinical pharmacovigilance experts to track and resolve safety events.

Patient safety is paramount to us and our clients.