Elevate clinical research as a Clinical Trial Associate specializing in regulatory tasks for Alzheimer trials. This role requires strong compliance acumen and keen organizational skills in a dynamic on-site environment.

Reporting to the Manager or Director, you will manage regulatory activities vital to supporting Alzheimer’s clinical trials. Your responsibilities will include preparing and submitting documentation, coordinating essential study materials, and ensuring adherence to regulations like ICH-GCP. Effective collaboration with teams will enhance the progress of ongoing studies.

Key Responsibilities:
• Prepare and submit regulatory documents to Ethics Committees
• Manage compliance with regulatory commitments
• Coordinate the collection of essential study documents
• Act as liaison for communication with sponsors
• Track training compliance among team members

Requirements:
• Minimum 2 years as a Regulator...