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RTI International

Senior Biostatistician

RTI International

. Plan, conduct, and document statistical analyses for observational studies and clinical trials, with an emphasis on causal inference methods.

Posted 4/21/2026full-timeBarcelona • 🇪🇸 SpainSeniorWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Plan, conduct, and document statistical analyses for observational studies and clinical trials, with an emphasis on causal inference methods.
  • Implement target trial emulation analyses using real-world data sources.
  • Develop simple to moderately complex statistical analysis plans and contribute to more complex SAPs under supervision.
  • Write statistical sections of study reports, protocols, and proposals.
  • Ensure the quality, accuracy, and timeliness of statistical analyses and programming outputs.
  • Provide statistical and methodological solutions to internal, cross-functional project teams.
  • Mentor and oversee less experienced staff on selected project tasks.
  • Learn and apply new statistical methods in response to evolving project and research needs.
  • Contribute to the scientific reputation and professional development of the biostatistics group and prepare presentations for external audiences.

Requirements

What you’ll need
  • Bachelor's Degree and 8 years of experience, Master's degree and 6 years of experience, PhD and 1 years of experience, or equivalent combination of education and experience.
  • Strong programming skills in R (required), including experience developing reproducible analysis pipelines.
  • Experience with causal inference methods (e.g., propensity score methods, weighting, marginal structural models); target trial emulation experience is desirable but not required.
  • Experience analyzing real-world data (e.g., claims, electronic health records, registries).
  • Familiarity with SAS, machine learning, and natural language processing is desirable but not required.
  • Background in biostatistics or related quantitative disciplines.
  • Knowledge of Good Clinical Practice (GCP), quality assurance principles, and regulatory environments.
  • Strong analytical, organizational, and problem-solving skills.
  • High level of written and verbal communication skills in English.
  • Ability to manage multiple tasks, meet timelines, and work effectively in collaborative team environments.
  • Experience in the pharmaceutical industry is a plus.

Benefits

Comp & perks
  • flexible work arrangements
  • professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
statistical analysescausal inference methodsRreproducible analysis pipelinesstatistical analysis plansreal-world data analysisSASmachine learningnatural language processingbiostatistics
Soft Skills
analytical skillsorganizational skillsproblem-solving skillswritten communication skillsverbal communication skillsmentoringcollaborationtime management
Certifications
Bachelor's DegreeMaster's DegreePhD