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Fortrea

Global CRO providing Phase I-IV trials

Statistical Programmer Intern

Clinical Research OperationsConfirmed live in the last 24 hours
InternshipMexico City, CDMX, MexicoNo salary listedRemote

About the Job

Requirements

  • Must be a student at Universidad Panamericana, Universidad Intercontinental, or Tecnologico de Monterrey.
  • Must be a student in relevant studies; a Bachelor of Science in engineering, computing, mathematics, computer science, programming, statistics, public health, or a related field is required. Relevant and equivalent experience may be considered in lieu of educational requirements.
  • Must be able to organize and communicate effectively.
  • Must demonstrate attention to detail.
  • Must be able to work well with others.
  • Must deliver consistent, high-quality work.
  • Must be able to use a computer and departmental tools.

Responsibilities

  • Ensure that all data management activities comply with relevant regulatory requirements and Good Clinical Practice.
  • Follow applicable departmental Standard Operating Procedures and Work Instructions.
  • Complete required trainings according to timelines.
  • Generate, review, and action queries on an ongoing basis to address inconsistent data identified during data review activities, and ensure proper modification or correction is made to the database.
  • Work on assigned data management-related tasks.
  • Assist with validation of the Electronic Data Capture system and/or SAS listings against study specifications and User Acceptance Testing, as required, according to the Electronic Data Capture User Acceptance Testing Checklist.
  • Assist with creating and reviewing data management documents as required, such as the Data Management Plan, Edit Check Specifications, and Vendor Data Plan.
  • Review reports and take actions as defined in the Data Management Plan and/or Data Review Plan.
  • Perform ongoing and final consistency checks and review data listings as defined in the Data Management Plan and Data Review Plan.
  • Assist with decommissioning and archiving tasks, generate and distribute reports, and perform other ad hoc tasks as required.
  • Perform other duties as assigned by the study and/or line manager.

Desired Qualifications

  • English language skills, both written and oral.
  • Working toward a bachelor's or master's degree in a life science subject.
  • Experience delivering multiple projects in an academic setting.
  • Ability to collaborate with various stakeholders and internal and external colleagues.
  • Ability to embrace diverse ways of thinking through various forms of collaboration and partnership.
  • Additional languages.

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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