Clinical Research Job at Fortrea, Toronto | Life Sciences | Apply Now
First-in-human clinical trials are the critical frontline of global drug development. If you are looking to advance your career by supporting these cutting-edge early-phase studies, this remote Project Coordinator position at Fortrea is a high-impact Clinical Research Job. For professionals eager to build a long-term Fortrea career, this role offers a direct pathway to mastering the full lifecycle of clinical trial management.
- Job Position: Project Coordinator, Early Phase Clinical Research – Canada
- Location: Toronto (Remote)
- Job requisition ID: 262526
About the Company
Fortrea is a leading global Contract Research Organization (CRO) renowned for its scientific rigor and decades of clinical development experience. Operating in over 90 countries with more than 19,000 staff members, Fortrea transforms drug and device development for partners across 20+ therapeutic areas. Taking on this Life Sciences Job means you will work alongside experienced project managers and cross-functional teams to help bring new therapies to patients—starting from their very first step into clinical trials.
Clinical Research Job – Key Responsibilities
As a Project Coordinator, you will serve as the organizational anchor for Phase I clinical trials. You are responsible for keeping studies strictly on track, fully compliant, and consistently audit-ready.
Your day-to-day duties in this Clinical Research Job will include:
- Study Delivery: Coordinate and support the seamless delivery of Phase I clinical trials, including managing complex external site studies.
- Document Management: Develop, update, and maintain key study documents, including comprehensive project plans, communication plans, and risk registers.
- Timeline Tracking: Rigorously track project timelines, study milestones, and overall study progress to ensure successful, on-time execution.
- System Compliance: Manage essential trial systems, such as the Clinical Trial Management System (CTMS) and electronic Trial Master File (eTMF), ensuring total accuracy and regulatory compliance.
- Meeting Leadership: Lead and support internal and external study meetings by preparing agendas, taking precise minutes, and tracking follow-up actions.
- Operational Support: Act as the key point of contact for internal teams and external sites, supporting feasibility assessments, start-up activities, and vendor coordination.
- Team Development: Contribute to continuous improvement initiatives and help mentor junior team members as you grow in your role.
Candidate Profile Required For Clinical Research Job
To secure this competitive Life Sciences Job, you must bring a strong blend of early-phase clinical knowledge and exceptional organizational skills.
- Educational Foundation: A degree in life sciences or a related field (or equivalent proven industry experience) is required.
- Required Experience: 2 to 3 years of clinical research experience, with a strong preference for candidates who have worked directly in early-phase (Phase I) studies.
- Operational Background: Proven experience actively supporting project management or clinical study coordination.
- Regulatory Mastery: A solid, working knowledge of GCP (Good Clinical Practice) and ICH guidelines, alongside standard clinical trial processes.
- Core Competencies: Strong organizational, written/verbal communication, and problem-solving skills to navigate a fast-paced environment.
In summary, this Project Coordinator role is a definitive stepping stone for professionals aiming to specialize in early-phase clinical trials. By securing this Clinical Research Job, you will gain unparalleled exposure to the entire trial lifecycle within a massive global CRO. Because the application window closes on May 21, 2026, apply immediately to secure your chance at a deeply rewarding Fortrea career.
