Our dedicated Clinical Research Associates (CRAs) monitors each
study. Each CRA have therapeutic knowledge and they are trained in
patients management, investigative sites management and specific
challenges involved in trial. All Clinical Trial Monitoring team members
receive ongoing training to ensure they are completely up to date with
current regulatory, project management techniques and technologies
involved in Managing the clinical trials. They are supported by our
inhouse project Managers and Clinical Operations Management
Our Monitoring group supports sites, site team and patients,
overseeing the running of studies and directing strategy throughout the clinical trial phase and process. The group acts as a bridge between
the Site team and Customer Project group or Project Manager, they will
be playing a central role in developing trial processes, and driving
solutions around data-focused monitoring, as well as predicting any
issues that may arise and work with sites, COM and Customer to
mitigate the challenges.
We have equipped to offer clinical monitoring capabilities in either a full
service or FSP model and our monitoring team engages a hands-on
partnering approach that synergize collaboration and communication
between assigned CRAs, investigative sites, cross-functional teams,
line management and customers.
We offer site assessment and qualification to study close-out, our
commitment to success starts with strategic collaboration.
Syncorp Clincare prepares CRAs with study-specific training and who are familiar with regulatory requirements, Project specifics, SOPs, Guidelines and cultural knowledge helps to manage site workflow, reduce investigator burden, improve data quality and accelerate database lock.