Clinical Outcomes Solutions
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.
Principal Biostatistician
Job not on LinkedIn
🔥 23 hours ago
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Clinical Outcomes Solutions
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.
📋 Description
• Lead statistical activities for assigned Clinical Trials (Phases 1 to 2) independently from protocol design to reporting of results. • Represent Statistics function on cross-functional trial (and possibly indication / project) teams and collaborate effectively with all cross-functional stakeholders. • Oversight of internal programming activities and/or CRO contributions on assigned clinical trials and other activities. • Contribute to or lead other activities from a statistical perspective as appropriate, including but not limited to Safety Reporting, ISS/ISE, addressing questions from Health Authorities, Publications. • Use SAS and/or R for purposes like QC of datasets and deliverables, inferential statistical analyses, modelling/simulation, exploratory analyses etc. • Contribute to and participate in other initiatives at Cytel or sponsor side as appropriate. • Oversight of more junior Statisticians as required.
🎯 Requirements
• 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)
🏖️ Benefits
• Health insurance • Professional development • Training and support
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