Project Coordinator I

Posted 21 Days Ago
Be an Early Applicant
São Paulo, BRA
In-Office
Junior
Biotech
The Role
Supports clinical project leads with study schedules, budgets, vendor and contract tracking, risk and issue management, quality compliance, audit preparation, team communications, documentation, and lessons-learned tracking. Maintains project systems and trackers, coordinates meetings and collaboration tools, monitors timelines and action items, and escalates risks or out-of-scope work. The role is part of a structured project management development program and requires 0–2 years of relevant experience.
Summary Generated by Built In

Job Overview:

    The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Project Coordinator-I performs the essential duties with a large degree of guidance and support from the Fortrea web of support that includes, but is not limited to, the Project Lead(s), Line Manager, mentor, and subject matter experts. As s/he progresses along the learning curve, the Project Coordinator I may mentor other PM Academy PCs in some areas of expertise.

Summary of Responsibilities:

    Operational Delivery:
  • TIME: Work with project team to set up and maintain project schedule. Update timelines within MS Project, CTMS, project governance tool, and other trackers. Escalate when timelines are at risk.
  • COST: Work with Project Lead to assist with TAQ/TAR (timesheet vs budget) reviews; vendor financial tracking and reconciliation; sponsor contract financial tracking and reconciliation; and final project financial reconciliation.
  • SCOPE: Work with Project Lead to conduct Contract vs Study Plan Review. Maintain tracker of out of scope (OOS) work performed. Assist the Project Lead to create Change Order Forms. Provide vendor management, escalating OOS activities to Project Lead.
  • RISK: Update Xcellerate Risk Identification and Issue Resolution (RIIM) tool; and follow outstanding action items to resolution. Ensure Xcellerate Risk Assessment Categorization Tool (RACT) is complete, using Xcellerate Risk library. Work with Study Team to ensure Protocol Deviations are updated in Xcellerate RIIM.
  • QUALITY: Update Project Governance Tool monthly. Support the study team to identify, prevent and close quality compliance gaps. Support the Project Lead to prepare for audits and/or investigations, including creation of story boards to document issues that may occur during the study. Support study team to ensure timely closure of audit/inspection CAPAs.
  • TEAM COMMUNICATION: Facilitate study team communication and collaboration by attending and setting up team meetings; updating the ADI log; updating the Task Order Matrix; maintaining the Project Directory; setting up distribution lists, SP sites, mailboxes, and other collaboration tools; and set up / maintain project-specific trackers.
  • TEAM COLLABORATION: Collaborate with other support functions to facilitate timely TMF uploading, TMF reviews, TMF issue resolution, systems access, project specific training curriculum, and other delegated tasks. Monitor for, escalate, and help to enforce redaction of subject sensitive information and identifiers in any study documentation.
  • LESSONS LEARNED: Work with Study Team to maintain Lessons Learned tracker.
  • OTHER: And all other duties as needed or assigned

Qualifications (Minimum Required):

  • 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

Experience (Minimum Required):

  • 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.

Physical Demands/Work Environment:

  • Standard Office.
  • 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

Learn more about our EEO & Accommodations request here.

Skills Required

  • University or college degree, preferably in life science, or certification in a related allied health profession from an appropriately accredited institution
  • Three or more years of relevant clinical research, pharmaceutical, CRO, or healthcare experience may substitute for the education requirement
  • Relevant and equivalent experience may be considered in lieu of educational requirements
  • 0–2 years of relevant industry experience
  • Knowledge of ICH Guidelines and Good Clinical Practice, including international regulatory requirements for clinical development programs
  • Computer competency with Microsoft Word, Excel, Project, Access, and PowerPoint
  • Ability to develop accurate study-related documents with minimal supervision
  • Ability to communicate verbally and in writing
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The Company
HQ: Durham, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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