Project Coordinator I

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🔥 12 hours ago

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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 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

• 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

• 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.