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Fortrea

Project Coordinator

Fortrea

. Work with the project team to set up and maintain project schedules; update timelines in MS Project, CTMS, project governance tools, and other trackers; escalate timeline risks .

Posted 9/24/2026full-timeRemote • Mexico, Brazil, Colombia, ArgentinaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in project management and financial tracking within clinical research, utilizing tools such as MS Project and Xcellerate for risk management and compliance. Proficient in communication and collaboration to support study teams and ensure adherence to regulatory standards.

Highest-signal resume keywords
Project ManagementFinancial TrackingRisk ManagementClinical Research ExperienceRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project SchedulingFinancial ReconciliationRisk AssessmentProtocol Deviation ManagementDocument Development
Soft Skills
Verbal CommunicationWritten CommunicationFlexibility
Tools & Technologies
MS ProjectXcellerate RIIMXcellerate RACTMicrosoft WordMicrosoft Excel
Certifications & Qualifications
University/College DegreeCertification in Allied Health Profession
Industry Keywords
ICH GuidelinesGCPClinical Development ProgramsCROPharmaceutical

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Work with the project team to set up and maintain project schedules; update timelines in MS Project, CTMS, project governance tools, and other trackers; escalate timeline risks
  • Assist the Project Lead with timesheet-versus-budget reviews, vendor financial tracking and reconciliation, sponsor contract financial tracking and reconciliation, and final project financial reconciliation
  • Conduct Contract versus Study Plan Reviews with the Project Lead; maintain out-of-scope work trackers; assist with Change Order Forms; provide vendor management and escalate out-of-scope activities
  • Update the Xcellerate Risk Identification and Issue Resolution (RIIM) tool and follow action items through resolution
  • Complete the Xcellerate Risk Assessment Categorization Tool (RACT) using the Xcellerate Risk library
  • Ensure Protocol Deviations are updated in Xcellerate RIIM
  • Update the Project Governance Tool monthly
  • Support identification, prevention, and closure of quality compliance gaps
  • Support audit and investigation preparation, including creation of issue storyboards
  • Support timely closure of audit/inspection CAPAs
  • Facilitate study team communication and collaboration through meetings, ADI logs, Task Order Matrix, Project Directory, distribution lists, SP sites, mailboxes, collaboration tools, and project-specific trackers
  • Collaborate with support functions on TMF uploading, TMF reviews, TMF issue resolution, systems access, project-specific training curricula, and delegated tasks
  • Monitor, escalate, and help enforce redaction of subject-sensitive information and identifiers in study documentation
  • Maintain the Lessons Learned tracker with the Study Team
  • Perform other duties as needed or assigned

Requirements

What you’ll need
  • University/college degree (life science preferred), or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from appropriately accredited institution
  • In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements
  • 0-2 years of relevant industry experience
  • Knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs preferred
  • Computer competency with various programs (e.g., Microsoft Word, Excel, Project, Access and Power Point)
  • Ability to develop accurate study related documents with minimal supervision
  • Ability to communicate verbally and in writing
  • Must be able to work at a computer keyboard 6-8 hours per day
  • Must be flexible to accept changes in work assignments, as business needs require