Site ICRA I<\/p>\n
Maple Grove, MN<\/p>\n
On-Site Role<\/p>\n
$40 – $43 per hour<\/p>\n
11-month contract (likelihood of extension)<\/p>\n
Our client, a large medical device company, is seeking a Site ICRA I to participate in the planning and execution of clinical studies at assigned study sites in Maple Grove, MN. This role is responsible for supporting timely site activation, ensuring compliance with study protocols, domestic and international Good Clinical Practices, applicable regulatory standards, and Standard Operating Procedures throughout the study lifecycle. The Site ICRA I will collaborate closely with field staff and in-house personnel to manage study start-up, maintenance, and close-out, review informed consent documents, analyze study data, resolve data queries, and address findings from monitoring visits and audits. The position also serves as a primary contact for assigned study sites, facilitates communication, and supports process improvement activities. The role requires strong communication, organizational, and analytical skills, proficiency in Microsoft Office Suite, and the ability to work independently. Familiarity with clinical trials research processes and professional certification are considered desirable. This is an 11-month contract with the likelihood of extension.<\/p>\n
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