- Responsible for planning, managing and execution of statistical deliverables in clinical trial and non-trial activities in the project
- Responsible for providing statistical input to authority required documents or meetings
- Responsible for ensuring that clinical trial and non-trial tasks are aligned with the project specifications
- Deliver results through and ensure understanding among colleagues relevant for problem-solving
- Lead project teams to achieve milestones and objectives
- Prioritize, plan, manage and execute Clinical Trials and submissions within project area
- Mentor and develop successors within project area
- Fully responsible for statistical methodology and deliverables within the project
- Main contact to stakeholders regarding statistics within the project
- MSc. in statistics or equivalent
- +3 years of experience as a statistician within the pharmaceutical area or equivalent knowledge through relevant experience
- Experience with a broad range of statistical tasks
- In-depth knowledge of biostatistical methods
- Extensive experience with practical applications of biostatistical methodology
- In-depth knowledge of drug development
- Broad experience with statistical software and IT and in-depth experience with at least one statistical software package
- Good knowledge of GCP and statistical guidelines within drug development
- Regular experience with communication of statistical issues and presentations
- Basic understanding of the pharmaceutical industry and key elements of the value chain, with a focus on immediate stakeholders and how to deliver on own goals
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Biostatistician - London, United Kingdom - Lifelancer
Description
About the role
ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What you will be doing:
You are:
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