Fortrea

Fortrea

Project Coordinator I, Phase I

Durham

No sponsorship$15k-$20kDetected 1 day ago
GCPProject ManagementClinical TrialsClinical ResearchMedical DevicesResearchCommunicationProblem Solving

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odds of building a lasting career here

15Unrated
Cap-exempt (no lottery)0
Sponsors this role0
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

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About the role

  • Our Phase I team is currently seeking Project Coordinator I to join their growing group!
  • All candidates must reside in the United States.
  • 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.

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).
  • 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.

Requirements

  • 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.
  • Varied hours may be required.
  • 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.
  • 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.
  • 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.
  • Note: This role does not provide sponsorship.
  • Work Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.

Compensation

  • $28-30 USD per hour

Equal opportunity

  • Learn more about our EEO & Accommodations request here.

Visa & Work Authorization

  • Note: This role does not provide sponsorship.
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This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.