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CTI Clinical Trial and Consulting Services is seeking a CRA to act as the main CTI contact for assigned study sites and to conduct site visits (PSV, SIV, IMV, COV) while ensuring quality and regulatory compliance. You will support study start-up activities, feasibility assessments, and site selection, collecting essential regulatory documents and participating in team meetings.
The role requires 3–5 years of clinical research experience as a CRA or related field, a life science background, and
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