Clinical Research Associate I - Trials Monitoring
Allen Spolden
Denver-based clinical research support professional sought to assist the clinical study team with protocols, site evaluations, and regulatory documentation. Responsibilities include site initiation visits, monitoring, report preparation, and archive maintenance, all while adhering to GCP and regulatory standards. Requirements include a BA/BS or RN/BSN or equivalent, 1–2 years of clinical research experience, and strong written and verbal communication skills. #J-18808-Ljbffr Allen Spolden
Vacancy posted 3 days ago
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