Senior Clinical Trial Monitoring Lead
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ICON in Pennsylvania is seeking a Sr. Clinical Research Associate to lead clinical trial monitoring and ensure compliance with protocols and regulations. The ideal candidate will have a Bachelor's degree and extensive experience in clinical trials. Responsibilities include monitoring sites, conducting visits, and collaborating with teams to ensure data integrity. ICON offers various benefits including health insurance, retirement planning, and a commitment to an inclusive workplace. Ideal for those who enjoy diverse environments and fostering compliance in clinical operations. #J-18808-Ljbffr ICON
Vacancy posted 2 days ago
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