A clinical research coordinator plays a significant role in clinical trials and studies, performing multiple activities and fulfilling various responsibilities.
They are a key person of interest in any trial, whether it’s for a drug, medical tool, or device, and remain involved from start to finish. A significant responsibility that they bear is patient safety and coordination, making them indispensable to the research process.
Among the many factors that make them key players in the process, here’s a brief overview of their importance:
Clinical research coordinators help in recruiting patients and volunteers
One of the primary functions of a clinical research coordinator is to bring participants and patients on board. This involves designing and determining what patient or participant population plan to target (based on the nature of the drug, critical data points, and aims of the study), and more.
Additionally, they also screen participants, checking them for eligibility criteria and ensuring that they meet all requirements, qualify for the study, and have clearance.
Obtaining explicit, clear, informed consent from them
As part of their recruitment process, they must also obtain explicit, clear, and written informed consent. This also extends to patients or participants whose ability to consent may be compromised. You can streamline that through eConsent forms and eCRFs for clinical trials and use our software programs to make work easier.
Maintaining participant safety during the trial process
As a clinical research coordinator, one of the most important roles is to ensure participant and volunteer safety. Not only does it involve finding ways to protect their confidentiality and privacy, but also monitoring symptoms, signs of reactions, and other risks they’re faced with.
Managing data collection and quality control using EDC software
Clinical research coordinators work with multiple stakeholders and personnel, including the lead investigator, to collect and manage data, improve quality control, and ensure that everything is in order. They do this by creating better forms, sharing forms with participants, monitoring their safety and health requirements, and entering the information they collect into EDC software programs for clinical trials.
Clinical research coordinators perform a wide range of roles and functions for clinical trials, and our EDC software can help streamline their work. The software offers a variety of features and functions, including rapid study design, data entry and collection, and data analysis and management.
Learn more about our services and software programs here or sign up for a free demo to get an overview of its features.
