Clinical Research Associate

• Conduct site visits within the select region
• Perform monitoring activities to ensure adherence to compliance standards with study protocols, regulatory requirements, and GCP
• Work closely with site staff to ensure proper documentation and data collection
• Support study start-up, maintenance, and close-out activities
• Maintain effective communication with study teams and stakeholders
• Provide updates and reports on site performance and study progress

• Experience in Clinical research, preferably within a CRO or pharmaceutical setting
• Previous history of independent monitoring experience is required
• Background in diabetes or obesity therapeutic areas is beneficial but not essential
• Strong organizational and communication skills
• Capacity to travel regionally as the business requires
• Academic candidates with relevant experience, including monitoring, will also be considered

Background in diabetes or obesity therapeutic areas