Project Coordinator I

🕒 July 31

🇺🇸 United States – Remote

💵 $28 - $35 / hour

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

👻 Ghost score 50%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Coordinate and support delivery of Phase I clinical trials, including external site studies • Develop and maintain project plans, communication plans, and risk registers • Track timelines, milestones, and study progress • Lead and support study meetings, including agendas, minutes, and follow-up actions • Manage CTMS and eTMF systems for accuracy and compliance • Serve as a key contact for internal teams and external sites • Support feasibility, start-up activities, and vendor coordination • Contribute to continuous improvement initiatives • Help mentor junior team members • Drive occasionally to site locations and travel domestically and internationally as needed

🎯 Requirements

• 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 • All candidates must reside in the United States • No sponsorship provided • Ability to access and use in-house and off-the-shelf computer software • Regular and consistent attendance • Varied hours may be required • Ability to lift and carry 15–20 lbs

🏖️ Benefits

• 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 • Career growth within a global clinical research organization • Occasional domestic and international travel • Ongoing applications accepted