On-Site Coordination (CRC)
Key operational support at the heart of investigator sites
Clinical Research Coordinators (CRCs) play a central role in the day-to-day management of studies at investigator sites. Pharmaspecific provides experienced CRCs to support medical teams and optimise the operational management of studies.
With their expertise and rigour, our clinical research coordinators contribute to data quality, adherence to procedures and a smooth experience for investigators and participants alike. They also take part in clinical study coordination, providing an operational link between site teams and all project stakeholders. Their presence makes it easier to track activities, collect clinical information and maintain the documentation needed for studies to run smoothly.
This organisation supports structured clinical study management and better continuity of activities at sites. Our clinical research coordinators can notably support data collection, eCRF completion and the follow-up of information collected during visits, while reducing the operational workload of hospital teams.
Project management thus benefits from close, hands-on support that promotes the quality, reliability and consistency of the data collected.
A daily presence to support your studies
Our Clinical Research Coordinators (CRCs) work directly at investigator sites to ensure the operational follow-up of studies and support teams with routine activities. They contribute to clinical data collection and entry, the tracking of study documents and the coordination of all actions required for the protocol to run smoothly. Their presence also facilitates communication between medical teams, investigators and research teams. This organisation promotes smooth, rigorous clinical study management and better quality of the data collected.
Rigorous, reliable support
We ensure the implementation of procedures, document tracking and visit coordination to guarantee compliance and data quality.
Our clinical research coordinators also ensure that activities at investigator sites are well organised, facilitate the flow of information and regularly follow up on everything the study requires. This organisation supports structured clinical study management and effective clinical study coordination. They also help follow up on information collected during visits and keep the documents needed for the study up to date.
Their involvement facilitates communication between all stakeholders and helps maintain continuity of activities at investigator sites.
A trusted link with patients
Our Clinical Research Coordinators (CRCs) play an active role in welcoming, following and supporting participants throughout their study journey, ensuring that procedures are followed and that the information collected is of high quality.
Our services include
Need CRC support for your studies?
Our teams are available to discuss your needs and offer resources tailored to your projects.