Clinical Trial Operations Coordinator

Fortrea; Durham (NC); On-site; USD 45,000 - 50,000; Full time

Job summary

Fortrea is seeking a Clinical Trial Administrator (CTA) to join the Clinical Project Team. The CTA will perform study-related administrative tasks, maintain TMF documentation, and support project team communications to ensure timely, high-quality clinical data production.

The role emphasizes adherence to SOPs, regulatory standards, and effective coordination with sites, sponsors, and internal team members. Strong organizational and proofreading skills are essential in a fast-paced environment.

Qualifications

• Bachelor's degree in the life sciences or an related field is required, or an Associate degree with 2 years of relevant experience.
• Fluent in English and the local language (speaking).
• Good reading/writing skills in English and the local language.

Responsibilities

• Document and track study activities using forms and project systems.
• Assist in preparation of study materials and site materials per SOPs.
• Take minutes and manage documentation for sponsor calls and meetings.
• Maintain tracking systems for study supplies and the TMF.
• Coordinate with vendors for study materials and study-related shipments.
• Generate reports as needed (e.g., CTMS site contact lists).

Skills

Communication skills

Organizational skills

Attention to detail

Proofreading

Time management

Education

Bachelor's degree in life sciences

Associate degree in life sciences (plus 2 years experience)

Job description

Fortrea is seeking a Clinical Trial Administrator (CTA) to join the Clinical Project Team. The CTA will perform study-related administrative tasks, maintain TMF documentation, and support project team communications to ensure timely, high-quality clinical data production.

The role emphasizes adherence to SOPs, regulatory standards, and effective coordination with sites, sponsors, and internal team members. Strong organizational and proofreading skills are essential in a fast-paced environment.