Our CRAs are chosen for their experience in clinical research and the appropriate therapeutic area.
As the crucial interface between the project team and the Investigator, CROMSOURCE CRAs demonstrate high levels of site management skills to ensure that issues at sites are addressed quickly and completely, allowing sites to work efficiently and maximize data quality.
CROMSOURCE CRAs tend to be home-based and are strategically located to ensure local knowledge, language, and cultural understanding, as well as to reduce travel costs and increase efficiency.
CROMSOURCE makes training a priority and all our staff undertake a specific and personalized training program. This means you can rely on the quality of CRAs assigned to your study.
CROMSOURCE CRAs perform all activities related to pre-trial/qualification visits, initiation visits, interim monitoring visits, and closeout visits, ensuring compliance to the clinical investigation plan and all regulatory requirements. As noted, they also maintain strong and constructive relationships with investigative sites to ensure successful trial progress.
In addition to our full service offering, CROMSOURCE’s Staffing Solutions division, TalentSource Life Sciences, also provides teams of CRAs on a per project or Functional Service Provider (FSP) basis. More details on TalentSource is available at the following link www.talentsourcelifesciences.com.