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Alira Health is seeking a Clinical Research Associate to independently conduct and oversee clinical trial site monitoring activities while ensuring protocol compliance, quality, and regulatory adherence. The role manages site visits, monitoring documentation, data verification, investigator relationships, issue resolution, and CRA team support. Responsibilities Provides guidance, oversight, and feedback to the CRA te

Alira Health hires a Clinical Research Associate to conduct site monitoring and provide oversight, leadership, and guidance for clinical trials. The role supports protocol compliance, site training and recruitment, data integrity, and quality across study execution. Responsibilities Provides guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirement

Responsibilities Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, etc Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs Responds to sites’ regulatory board requests for protocol and ICF clarification as needed Ensures all required site regulatory documents and approvals