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Clinical Research Associate I (CRA I)

CND Life Sciences • Scottsdale, AZ, US • published 2026-10-14 08:32:16.617950

Description

**Position Summary** The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND’s Clinical Research Center site and investigator sites sponsored by CND or in collaboration with external partners. This role ensures that studies are executed in compliance with study protocols, Good Clinical Practice (GCP) R3 guidelines, budget constraints, and established milestone timelines. The CRA must have a strong understanding of clinical trial methodologies, regulatory requirements, and the ability to collaborate effectively with the investigators and internal and external cross\-functional teams. The CRA consistently upholds the highest standards of professionalism. **Job Responsibilities** * **Regulatory Compliance:** Ensure all clinical trials are conducted in adherence to the study protocol, ICH\-GCP guidelines, relevant regulations and SOPs. Manage central IRB tasks for participating sites from start\-up through close\-out. * **CND Site Subject Visits**: Assist providers with subject recruitment, scheduling and conducting site visits at the internal CND site as needed. Responsibilities may include obtaining informed consent (ICF), a...

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