Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of global clinical trials by providing essential operational and administrative support to study teams.

Key Responsibilities

• Support the coordination and tracking of clinical trial activities and documentation.
• Maintain Trial Master File (TMF) documentation and study tracking systems.
• Coordinate study materials, supplies, and shipment logistics.
• Assist with Investigator Meetings and project-related communications.
• Collaborate with study teams, investigative sites, sponsors, and vendors.
• Prepare reports and ensure accurate study records and data management.
• Provide overall administrative support to clinical project teams.

What We're Looking For

• Associate degree or equivalent qualification, or relevant clinical research experience.
• Previous administrative experience or exposure to the clinical research, pharmaceutical, or CRO industry.
• Strong written and verbal communication skills in English.
• Excellent organizational and time management abilities.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Detail-oriented with the ability to thrive in a fast-paced, matrix environment.

Why Join Fortrea?

• Contribute to innovative clinical research that improves patient lives worldwide.
• Work in a collaborative and supportive global environment.
• Enjoy opportunities for professional growth and career development.
• Flexible office-based or home-based working options.
• Limited travel requirements (up to 20%).