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Fortrea

Global CRO providing Phase I-IV trials

Adjudication Coordinator 2

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSão Paulo, State of São Paulo, BrazilNo salary listedIn-person

About the Job

Requirements

  • Meet one of the minimum qualification pathways: no degree plus 6 years of relevant or adjudication experience; an associate degree plus 4 years; a BS/BA degree plus 2 years; or RN with 0 years of relevant or adjudication experience.
  • Have a high degree of accuracy and close attention to detail.
  • Function as a strong team player.
  • Work efficiently with limited guidance.
  • Effectively balance multiple concurrent priorities.
  • Present and share useful business information across departments and functions.
  • Anticipate and identify problems and take appropriate corrective action.
  • Have strong written and verbal communication skills.
  • Have knowledge of medical terminology.
  • Have knowledge of hospital documentation practices.
  • Have knowledge of Good Clinical Practice (GCP).
  • Have accurate math and spelling skills, preferably with an aptitude for handling and proofreading numerical data.
  • Have good keyboard skills; knowledge of Microsoft Office and Windows applications is beneficial.
  • Speak, write, and read English and the local language.

Responsibilities

  • Operate in accordance with the Adjudication Services Operational Plan for assigned projects.
  • Process adjudication events, including maintaining event tracking systems; intake and triage; event linking and deactivation; tracking; data entry; document processing, including redaction of specified content; reviewing incoming event information for completeness and accuracy; identifying missing required data or documents; generating, reviewing, and closing or reissuing queries.
  • Contact site personnel to obtain missing data or documents.
  • Escalate open events for issue resolution and closure in accordance with the applicable Escalation Plan.
  • Complete First Review or Second Review QC Checklists as appropriate and assemble dossiers.
  • Conduct event reconciliation processes.
  • Coordinate implementation of adjudicator workflows, including disagreement resolution, re-review and re-adjudication, processing requests for additional documentation, and processing notifications of potential unreported events.
  • Prepare event adjudication status reports and metrics.
  • Conduct adjudication committee compilation processes, including identifying and screening potential adjudicators and collecting signed Confidentiality Disclosure Agreements, CVs, completed Adjudicator Selection Questionnaires, and signed contracts from potential adjudicators.
  • Provide mentoring and quality control for less experienced Adjudication Services staff, as appropriate.
  • Work in accordance with the Standard Operating Procedure system, including departmental Work Instructions.
  • Build and maintain working relationships within Adjudication Services and across functional units.
  • Perform other duties as assigned by management.

Desired Qualifications

  • A degree in one or more of the following disciplines is preferred but not required: Biological Sciences, Pharmacy, Nursing, Life Sciences, or Chemistry.
  • Knowledge of Microsoft Office and Windows applications is beneficial.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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