About The Position

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 Canada.

Requirements

  • Degree in life sciences or related field (or equivalent experience).
  • 2–3 years of clinical research experience, ideally in early phase studies.
  • Experience supporting project management or study coordination.
  • Knowledge of GCP/ICH guidelines and clinical trial processes.
  • Strong organizational, communication, and problem-solving skills.

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.

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.
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