Project Coordinator I, PC Academy

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

Our PC Academy is currently seeking a Project Coordinator I to join their growing group! All candidates must reside in the United States. As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Join a team where your work directly supports first-in-human clinical trials and the development of new medicines. As a Project Coordinator, you’ll play a critical role in keeping studies organized, on track, and audit-ready - working alongside experienced project managers and cross-functional teams in a fast-paced, collaborative environment. Remote based in United States.

What You’ll Do

• 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.

What You Bring

• 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.

Why Join Us

• 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.

Work Environment

Work is performed in an office environment with exposure to electrical office equipment.

Occasional drives to site locations with occasional travel both domestic and international.

Physical Requirements

• Frequently stationary for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Note: This role does not provide sponsorship.

Target Pay Range: $28-35 USD per hour

Learn more about our EEO & Accommodations request here.

At Fortrea, we’re all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence.

Regardless of your role, we’re all family, working together to achieve extraordinary results.

At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.