Project Coordinator I

Fortrea

Project Coordinator assisting with Phase I clinical trials in a global CRO environment. Collaborating with experienced teams and maintaining project organization and compliance.

Posted 7/31/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-Level💰 $28 - $35 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating Phase I clinical trials, managing study documentation, and ensuring compliance with GCP/ICH guidelines. Proven ability to track project timelines and mentor junior team members while maintaining effective communication with internal and external stakeholders.

Highest-signal resume keywords

Clinical Research ExperienceProject Management SupportGCP/ICH Guidelines KnowledgeCTMS ManagementStudy Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesProject Plans DevelopmentRisk Registers MaintenanceTimeline TrackingStudy Progress Monitoring

Soft Skills

Organizational SkillsCommunication SkillsProblem-Solving Skills

Tools & Technologies

CTMSETMF

Industry Keywords

Phase I Clinical TrialsFeasibility SupportVendor CoordinationContinuous Improvement Initiatives

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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.
Strong organizational, communication, and problem-solving skills.

Benefits

Comp & perks

Work on cutting-edge early phase studies at the forefront of drug development
Collaborate with experienced teams in a high-impact, fast-paced environment.
Gain exposure to the full lifecycle of clinical trials.
Grow your career within a global clinical research organization.
Be part of the team that helps bring new therapies to patients—starting from their very first step into clinical trials.