About this role
Clinical Trial Administrator (CTA)
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%).
Experience (Minimum Required):
• Minimum one (I) year administrative experience or equivalent training. • Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint). • Aptitude for handling and proof-reading numerical data, some spreadsheet software competency.
Learn more about our EEO & Accommodations request here.