Site Management Associate I - Remote

Overview

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

In Short

• Be the main point of contact between site personnel and CRA.
• Serve as the primary contact point for vendors and study supplies.
• Ensure pre-study testing is completed at local site facilities.
• Assist Monitors in completion of subject and site event information.
• Manage clinical supplies including order and inventory.
• Ensure regulatory and ethics committee submissions are up to date.
• Coordinate audits and inspections preparation and follow-up.
• Manage TMF and prepare Investigator Site Files.
• Arrange training for site teams in vendor-related systems.
• Ensure proper safety information flow with investigative sites.

Requirements

• College/University Degree in Life Sciences.
• Administrative work experience in international settings.
• Prior experience as CTA for CROs.
• Experience in Clinical Research.
• Knowledge of local regulations.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to work in a dynamic team environment.
• Strong communication and collaboration skills.

Benefits

• Advance your career in clinical research.
• Coordinate a variety of tasks and learn new things.
• Grow with the company.