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Principal Biostatistician

2 months ago


London, Greater London, United Kingdom Warman O'Brien Full time
Job Summary

We are seeking a highly skilled Senior Biostatistician to join our team at Warman O'Brien. As a key member of our Statistical Operations management team, you will be responsible for managing clinical trial programs and projects from start to finish.

Key Responsibilities
  • Program Management: Collaborate with our leadership team to oversee clinical trial programs and projects, ensuring timely and successful delivery.
  • Statistical Oversight: Provide expert statistical guidance on study design, sample size estimation, statistical analysis planning, and data handling.
  • Team Leadership: Coach, mentor, and develop less experienced Biostatisticians and Statistical Programmers, providing technical review and advice.
  • Protocol Design: Contribute to the development of trial protocols and research proposals, ensuring sound statistical methodologies.
  • Data Management: Review and provide input on clinical data management deliverables, including eCRFs, data validation specifications, and Data Management Plans.
  • Statistical Analysis: Perform hands-on statistical analysis and modeling, maintaining expertise in state-of-the-art statistical methodology and regulatory requirements.
  • Quality Control: Review and confirm ADaM dataset specifications, and perform quality control activities on ADaM datasets.
  • Regulatory Compliance: Ensure all study-level and drug-program-level statistical and programming activities are conducted in compliance with relevant regulatory requirements.
  • Communication: Collaborate with medical and clinical trial personnel to publish trial results, and participate in the writing of abstracts, manuscripts, posters, and presentations.
Requirements
  • A Ph.D. degree in statistical science, mathematical analysis, or a related field.
  • OR A Master's degree in the above fields.