Engage with our proactive talent pool for Clinical Research Associates supporting our Clinical Monitoring team. This is an invitation for individuals at varying seniority levels seeking career advancement in clinical research.
As a Clinical Research Associate, you will engage in site management activities ensuring protocol compliance and data integrity. Your role may include training responsibilities, conducting site visits, and facilitating the startup of clinical trials while working closely with senior staff and stakeholders.
Key Responsibilities: • Support site management through various monitoring visits • Conduct data reviews to ensure regulatory compliance • Assist senior CRAs with training and oversight • Engage in study meetings and training for professional development • Maintain timelines and TMF documentation thoroughly