Project Coordinator I

Fortrea; São Paulo; Presencial; BRL 70 000 - 100 000; Tempo integral

Resumo da oferta

Fortrea in São Paulo is seeking a Project Coordinator I for our Project Management Academy to support the Project Lead with schedules, budgets, and governance. The role offers hands-on guidance in a learning environment and opportunities to mentor others as you grow.

You will help maintain timelines in project tools, assist with Change Orders and vendor tracking, and contribute to study documentation and audit readiness under supervision from experienced colleagues.

Qualificações

• University/college degree (life science preferred) or allied health certification.
• Three or more years of relevant clinical research experience will be considered.
• Fortrea may consider equivalent experience in lieu of education requirements.

Responsabilidades

• Set up and maintain project schedules with milestone tracking.
• Assist with TAQ/TAR reviews, vendor financial tracking, and contract reconciliation.
• Support Change Order forms and vendor management activities.
• Update risk and quality tools and assist audits preparations.
• Facilitate study team communication and maintain project documentation.

Conhecimentos

Verbal & written communication

Time management

Team collaboration

Formação académica

University/college degree (life science preferred)

Certification in allied health (optional)

Ferramentas

MS Word

Excel

Project

Access

PowerPoint

Descrição da oferta de emprego

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

• 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, elevate, 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

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