Remote Phase I Clinical Trials Coordinator

Fortrea; Durham (NC); On-site; USD 39,000 - 41,000; Full time

Benefits offered by this job

Remote work

Job summary

Fortrea is seeking a Project Coordinator I to join our Phase I team. This role supports early-phase clinical trials, coordinating delivery, maintaining study documents, and tracking timelines in a fast-paced, cross-functional environment.

Candidates should have life sciences background and 2–3 years of clinical-research experience, with knowledge of GCP/ICH and exposure to CTMS/eTMF; remote work within the United States is available.

Qualifications

• Degree in life sciences or related field (or equivalent experience).
• 2–3 years of clinical research experience, ideally in early phase studies.
• Experience supporting project management or study coordination.
• Knowledge of GCP/ICH guidelines and clinical trial processes.
• Strong organizational, communication, and problem-solving skills.

Responsibilities

• Coordinate and support delivery of Phase I clinical trials, including external site studies.
• Develop and maintain key study documents (project plans, communication plans, risk registers).
• Track timelines, milestones, and study progress to ensure successful execution.
• Lead and support study meetings, including agendas, minutes, and follow-up actions.
• Manage systems such as CTMS and eTMF, ensuring accuracy and compliance.
• Act as a key point of contact for internal teams and external sites.
• Support feasibility, start-up activities, and vendor coordination.
• Contribute to continuous improvement initiatives and mentor junior team members.

Skills

Project coordination

Organization

Communication

Problem-solving

Education

Life sciences degree or related field

Tools

CTMS

eTMF

Job description

Fortrea is seeking a Project Coordinator I to join our Phase I team. This role supports early-phase clinical trials, coordinating delivery, maintaining study documents, and tracking timelines in a fast-paced, cross-functional environment.

Candidates should have life sciences background and 2–3 years of clinical-research experience, with knowledge of GCP/ICH and exposure to CTMS/eTMF; remote work within the United States is available.