Join the team as a Clinical Site Activation Specialist I, focusing on the start-up of investigative sites in clinical trials. Ensure timely regulatory submissions and effective contract negotiations for successful project delivery.

This entry-level role requires overseeing site contracts, essential document collection, and adherence to quality standards under the guidance of project leads. You will be the main contact with regulatory authorities, ensuring compliance and timely approvals during the site's activation process.

Key Responsibilities:
• Manage essential document collection for site activation
• Monitor and report on financial aspects of projects
• Compile and submit documents to the Trial Master File
• Oversee local submissions and regulatory approvals
• Negotiate contracts and budgets with investigative sites

Requirements:
• Experience in clinical trial site activation preferred
• Knowledge of ...