Project Coordinator I

Fortrea; Colombia; Presencial; COP 37.368.000 - 56.052.000; Jornada completa

Descripción de la vacante

Fortrea seeks a Project Coordinator I for the Project Management Academy to support the Project Lead and study teams in clinical trials. You will learn to set up schedules in MS Project, track timelines, and assist with budgets and change controls.

This entry-level role focuses on mentorship, quality processes, and collaborative work within a regulated environment, with opportunities to grow professionally.

Formación

• University/college degree (life science preferred) or certification in a related allied health profession.
• Three (3) or more years of relevant clinical research experience in pharmaceutical, CRO industries or health care setting will be considered in lieu of education.

Responsabilidades

• Set up and maintain project schedules; update timelines in MS Project and governance tools.
• Assist with budget reviews, vendor tracking, and financial reconciliation.
• Support Change Order creation and vendor management; escalate out-of-scope work as needed.
• Update risk tools (RIIM) and ensure timely action resolution with IT and study teams.
• Support quality and audit readiness, including documenting issues and CAPAs.
• Facilitate study team meetings and maintain project communication channels.

Conocimientos

Project coordination

Timeline management

Communication

Documentation

Educación

Life science degree

Related certification

Herramientas

MS Project

CTMS

Xcellerate RIIM

Descripción del empleo

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, 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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