
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
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51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
• Lead statistical activities for assigned Clinical Trials (Phases 1 to 4) independently from protocol design to reporting of results. • Represent Statistics function on cross-functional trial teams and collaborate effectively with all stakeholders. • Oversight of programming activities and/or CRO contributions on assigned clinical trials. • Contribute to or lead statistical activities including Safety Reporting, ISS/ISE, and Publications. • Use SAS and/or R for QC of datasets, inferential statistical analyses, modelling/simulation, exploratory analyses etc. • Oversight of more junior Statisticians as required.
• Minimum of Bachelor's degree in statistics or a related discipline. • 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. • Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership. • Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours. • SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. • Knowledge of R programming (R Shiny/Python)
• An experienced Principal Biostatistician with a passion for clinical development and analysis • Lead Phase I-IV clinical studies across your region • Working remotely with the support of Cytel • Engage within a global pharmaceutical client for next-generation patient treatment • Statistical and development support for clinical trials
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