Clinical Trial Associate

• Provide comprehensive administrative support for clinical trial operations, including organizing, maintaining, and updating study documentation within the Trial Master File (TMF)
• Manage documentation processes to meet regulatory and compliance requirements and Good Clinical Practice (GCP) standards
• Assist with preparation, review, and submission of Institutional Review Board (IRB) documents
• Monitor adherence to study protocols and regulatory guidelines, identifying and addressing compliance gaps
• Support day-to-day trial operations and collaborate with cross-functional teams to resolve operational issues
• Track and manage study data, including Case Report Forms (CRFs), ensuring data integrity and timely system entry
• Monitor trial progress and performance metrics, communicate with study sites, draft status reports, and escalate issues
• Coordinate site communications and serve as a point of contact for inquiries and updates
• Perform additional tasks assigned by the Associate Director of Clinical Affairs

Explore Clinical Trial Associate at Shoulder Innovations. Review requirements and application details.