Clinical Trial Associate

Job Summary

A company is looking for a Clinical Trial Associate to support the planning, execution, and management of clinical trials.

Key Responsibilities

• Provide administrative and project support for Clinical Operations
• Assist in planning, initiation, and execution of clinical trials in compliance with regulatory requirements
• Coordinate communication between study sites, sponsors, CROs, and other vendors

Required Qualifications

• Current knowledge of FDA and ICH Guidelines, including Good Clinical Practices (GCP)
• Proficiency in Microsoft Office Suite; knowledge of MS Project and/or Smartsheet is a plus
• Experience in maintaining and organizing trial master files and essential documents
• Ability to monitor trial progress and ensure timely data collection and entry
• Experience with budgeting, invoicing, and financial tracking for clinical trials