SynRG Clinical Research Associates (CRAs) play a major role in the successful conduct of a study. An open and effective communication allows CRAs to provide support and training to the site staff securing patient safety, data quality, and maximizing patient enrolment.

SynRG operates in full compliance with international and local regulations, as well as with ethical and scientific standards. Our medical monitors and most CRAs are licensed physicians, fluent in English; they are recognized by the industry professionals for their outstanding reputation in customer service. CRAs work closely with the sites to ensure compliance with study protocols, industry standards, data collection and regulatory requirements. The CRAs are regionally located in major cities in order to reduce travel costs.

Our CRAs enjoy their profession, and this is reflected in all interactions with clients, colleagues, and site staff. Our CRAs perform the following duties:

• Site selection, initiation, and routine monitoring
• 24x7 help line with medical and technical support
• Site personnel training and guidance
• Assessing protocol compliance and data integrity
• Regulatory document review
• Review of accessibility and eligibility of subjects
• Resolution of queries with the sites
• Preparation of site visit reports and follow-up letters
• Following up on proper AE and SAE reporting
• Drug accountability
• Study close-out visits