Remote Phase I Clinical Trials Coordinator

FTINC Fortrea Inc.; North Carolina; Remote; USD 39,000 - 48,000; Full time

Benefits offered by this job

Remote work (US)

Job summary

Fortrea Inc. is seeking a Project Coordinator I to support Phase I clinical trials and keep studies organized and audit-ready. The role collaborates with project managers and cross-functional teams in a fast-paced, remote environment.

You will develop and maintain study documents, track timelines, lead meetings, and manage systems such as CTMS and eTMF to ensure accuracy and compliance. Candidates should have a life sciences degree (or equivalent), 2–3 years of clinical research experience, and

Qualifications

• Degree in life sciences or related field, or equivalent experience.
• 2–3 years of clinical research experience.
• Experience supporting project management or study coordination.
• Knowledge of GCP/ICH guidelines and clinical trial processes.

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 help mentor junior team members.

Skills

Organization

Communication

Problem-solving

Attention to detail

Education

Life sciences degree

Equivalent experience

Tools

CTMS

eTMF

Job description

Fortrea Inc. is seeking a Project Coordinator I to support Phase I clinical trials and keep studies organized and audit-ready. The role collaborates with project managers and cross-functional teams in a fast-paced, remote environment.

You will develop and maintain study documents, track timelines, lead meetings, and manage systems such as CTMS and eTMF to ensure accuracy and compliance. Candidates should have a life sciences degree (or equivalent), 2–3 years of clinical research experience, and