Research Monitoring
Our Research Monitoring team oversees clinical trials to global standards, safeguarding data integrity and participant safety. Partner with us for site visits, training, query resolution, and more.
The Research Monitoring team partners with our collaborators to discover better treatment outcome for patients by monitoring the study in accordance to global standards, ensuring the data integrity, safety and well-being of the study participants.
Our CRAs undergo regular training and certification by the Association of Clinical Research Professionals (ACRP) as part of our continuous skills enhancement. Learning is an integral part of our work to ensure we are kept abreast of the latest clinical trial knowledge, skills and abilities that is rapidly evolving in this landscape.
We understand the importance of a collaborative culture with the sites as this is crucial to ensure the high quality of the study results. All our CRAs have prior site experience, hence they have a proficient grasp of the issues and challenges at the sites. This enables us to develop strategic approaches to address respective issues that arise in each study conduct.
Our services:
Conducting on site visits including site initiation, monitoring visit and close out
Site training and support
Query resolution
Drug accountability
Source data verification and review
SAE report review