As an Entry-Level Site Activation Specialist I, you will support clinical trials by starting up investigative sites effectively and efficiently. Your role focuses on meeting regulatory requirements and timeline adherence for site activations.
In this position, you will oversee essential documents, contracts, and financial monitoring while serving as the main contact for regulatory authorities. Your contributions will ensure that local activities align with project budgets and quality objectives under the supervision of the SSU Country Manager.
Key Responsibilities:
• Facilitate the submission process for site activation
• Track milestones and provide updates on project timelines
• Maintain compliance with SOPs and work instructions
• Coordinate budget negotiations with investigative sites
• Compile required documents for the Trial Master File
Requirements:
• Experience in regulatory submissions and site activation
• Understanding of financial monitoring in...