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.