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Fortrea

Global CRO providing Phase I-IV trials

Lead Biostatistician

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeNo salary listedRemote

About the Job

Requirements

  • A graduate-level degree in a discipline-relevant area, such as biostatistics or statistics, economics, data science, epidemiology, health economics, pharmacy, or medical.
  • Demonstrated scientific and technical expertise in biostatistics.
  • Demonstrated success leading SAS programmers.
  • At least 5 years of experience in biostatistics, including clinical study experience and drafting statistical analysis plans, or doctoral-level education with at least 4 years of experience.
  • At least 2 years of experience managing project-team SAS programmers for delivery of results.
  • Ability to draft client deliverables and maintain client relationships.
  • Programming proficiency in SAS.
  • Understanding of CDISC standards.

Responsibilities

  • Lead development of biostatistical activities in client engagements, including research, planning, analysis, synthesis, and communication.
  • Support statistical credibility of study deliverables to regulators, payers, and health technology assessment bodies through study design and analytic execution under the direction of senior-level real-world evidence biostatisticians.
  • Support the pursuit of new and repeat business, strengthen key client relationships, and contribute to scoping and budgeting relevant activities on opportunities.
  • Lead internal innovation initiatives in response to market and client needs.
  • Contribute to publications and conference presentations in the area of expertise.
  • Apply and help improve non-interventional methods standards and best practices for study design, analytic reproducibility, and transparency.
  • Address client needs with appropriate study designs and statistical methods.
  • Lead design and analysis of studies using real-world data, including claims, electronic health records, registries, and linked or tokenized data, including target trial emulation and external or synthetic control arms.
  • Apply causal inference and confounding-control methods, including propensity score matching or weighting, inverse probability weighting, instrumental variables, difference-in-differences, and marginal structural models, with appropriate sensitivity and quantitative bias analyses.
  • Ensure alignment with regulatory frameworks and data standards.
  • Author statistical analysis plans, contribute to protocol design and estimand definition, and perform analytic quality control and reproducibility for engagement deliverables.
  • Manage project teams responsible for scoped activities; advise and redirect them as needed.
  • Deliver strategic, methodological, and conceptual expertise in client engagements.
  • Advise on relevant scientific or technical matters.
  • Communicate project findings clearly and persuasively to client scientific, regulatory, and payer audiences.
  • Contribute to cross-functional teams as needed for projects.
  • Set and maintain personal behavior and business ethics in line with company culture.
  • Cultivate a positive environment and build positive connections with colleagues.

Desired Qualifications

  • A doctoral-level degree may be preferred, with scientific or technical knowledge and know-how aligned with client expectations.
  • Applied biostatistics experience in non-interventional and health economics and outcomes research disciplines.
  • Strong business development and problem-solving skills.

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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