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healthcare

Posted 15 hours ago

Project Coordinator, Early Phase Clinical Research - Canada

at Fortrea

Toronto, CanadaRemote

Responsibilities

  • 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.
  • Support feasibility, start-up activities, and vendor coordination.
  • Grow your career within a global clinical research organization.

Requirements

  • What You Bring 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.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • 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.

Additional details

  • 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.
  • What You’ll Do Coordinate and support delivery of Phase I clinical trials, including external site studies.
  • Act as a key point of contact for internal teams and external sites.
  • Contribute to continuous improvement initiatives and help mentor junior team members.
  • 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.
  • 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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