Site Management Associate II at VirtualVocations

A company is looking for an In-House CRA II.Key ResponsibilitiesCoordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issuesAssist in the preparation and review of regulatory documents, ensuring compliance with GCP and applicable regulationsTrack site performance metrics, analyze data, and provide reports to enhance site management efficiencyRequired QualificationsBachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical researchExperience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelinesStrong organizational and project management skills, with the ability to handle multiple priorities and deadlinesExcellent analytical skills with a focus on maintaining high-quality standardsExceptional interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams