Enhance clinical research integrity as a proactive Clinical Research Associate. Drive compliance and data accuracy while fostering strong relationships with site teams in a flexible environment.
In this essential role, you'll be responsible for performing comprehensive site management and monitoring tasks to guarantee adherence to clinical study protocols. Your focus will include evaluating site performance, ensuring informed consent processes are appropriately followed, and documenting key activities. Your impact is vital in maintaining the quality and integrity of clinical trials.
Key Responsibilities:
• Conduct monitoring visits and site assessments
• Ensure proper documentation and tracking of trial activities
• Collaborate with site staff for compliance training
• Monitor investigational product handling and safety
• Prepare for audits and support readiness initiatives
Requirements:
• Bachelor’s degree or equivalent in a related field
• Understanding ...