Phase I Clinical Trials Project Coordinator

Fortrea; North Carolina; On-site; USD 28,000 - 37,000; Full time

Job summary

Fortrea in the United States is seeking an Associate Project Coordinator to support Project Management for low complex studies. You will help develop study documents, monitor timelines, and assist in TMF filing and eTMF quality checks.

You will work under supervision with senior staff, coordinate meetings, update trackers, and support site and sponsor communications across study activities. Bachelor degree required, English proficient, and one to two years in a research environment preferred.

Qualifications

• University/college degree in healthcare/scientific field preferred.
• 1–2 years of experience in a research environment.
• Knowledge of GCP/ICH Guidelines and Regulatory Authority Guidelines.

Responsibilities

• Coordinate and complete project tasks for low complex studies.
• Create and maintain study documents (e.g., Project Management Plan, Communication Plan).
• Develop trial management tools and monitor study timelines.
• Attend, schedule, and organize study meetings; distribute agendas and minutes.
• Assist with TMF/eTMF filing and QC tools; support document transfer to TMF.

Skills

English proficiency

Education

University degree

Job description

Fortrea in the United States is seeking an Associate Project Coordinator to support Project Management for low complex studies. You will help develop study documents, monitor timelines, and assist in TMF filing and eTMF quality checks.

You will work under supervision with senior staff, coordinate meetings, update trackers, and support site and sponsor communications across study activities. Bachelor degree required, English proficient, and one to two years in a research environment preferred.