Detail-oriented Clinical Research Professional with a foundation in Biological Engineering and practical experience in supporting the coordination and management of clinical trials. Skilled in documentation oversight, subject tracking, and maintaining regulatory compliance using tools like Veeva Vault, Oracle, and CRIO and EDC tools such as Medidata, Reihen, and Cube. Demonstrates strong organizational and communication skills essential for site coordination, issue tracking, and cross-functional collaboration. Eager to contribute to meaningful projects and grow within a dynamic and collaborative environment.
Experience: 5 - 10 years
Experience: 5 - 10 years
Experience: 1 - 2 years
Experience: 1 - 2 years
Experience: 2 - 5 years
Experience: 1 - 2 years
Experience: 1 - 2 years
“I had this VA that I could turn things over to made it a lot easier”
Kyle Mckenna
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