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Fortrea

Global CRO providing Phase I-IV trials

Real World Evidence - SAS Programmer, CDISC/SDTM Specs

Data AnalysisUpdated on Nov 10
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in statistics, mathematics, epidemiology, or another relevant field is required, although relevant and equivalent experience and successful project outcomes may be considered in lieu of the education requirement.
  • Proficiency in a relevant programming language that meets current client demand, such as SAS, R, or Python.
  • Proficiency in SAS macro language.
  • Working knowledge of Microsoft Word, PowerPoint, and Excel.
  • At least 3 years of health research data analysis experience.
  • Ability to solve problems independently and follow defined processes.
  • Strong attention to detail.
  • Strong oral and written communication.
  • Ability to work in an upright or stationary position for 6–8 hours per day, make repetitive hand, finger, and wrist movements to operate lab equipment, and occasionally crouch, stoop, bend, or twist the upper body and neck.
  • Ability to use a variety of in-house and off-the-shelf computer software.
  • Ability to lift, carry, or move light to moderate objects, including luggage and a laptop, up to 15–20 pounds.
  • Regular and consistent attendance.

Responsibilities

  • Provide programming for analyses of real-world data from observational studies and secondary sources, including claims, hospital administration, electronic health records, and registries.
  • Develop analysis-ready datasets from source data, derive analytic variables, and follow the analytic plan.
  • Independently develop tables, figures, and listings from analytic datasets in accordance with an analytic plan.
  • Program validation of analysis datasets and table, figure, and listing results, and resolve discrepancies with minimal oversight.
  • Create and maintain programming documentation for assigned deliverables.
  • Cross-check written deliverables against analytic results for quality.
  • Communicate accurate and timely status updates to real-world evidence biostatisticians, epidemiologists, and team members.
  • Provide analytic programming for other data sources on projects as needed.
  • Follow standard operating procedures relevant to assigned projects.
  • Identify opportunities to improve productivity, quality, and efficiency in analytic processes.
  • Provide informal guidance to Associate, RWD Analysts.
  • Participate in department meetings to share knowledge and insights.
  • Maintain personal behavior and business ethics consistent with Fortrea culture.
  • Contribute to repeat business through quality analyses and deliverables.
  • Perform other duties as needed or assigned.
  • Work occasional evenings and weekends as required to meet project deadlines.

Desired Qualifications

  • Experience conducting analyses of observational study data.
  • Proficiency in CDISC standards, including writing SDTM and ADaM specifications.
  • Experience applying CDISC standards to observational study data.
  • Analytic experience with secondary data sources, including claims, hospital administration, electronic health records, and registries.

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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