At a Glance
- Tasks: Lead statistical activities for clinical trials and collaborate with cross-functional teams.
- Company: Join a global pharmaceutical client with a focus on innovation.
- Benefits: Competitive salary, professional development, and the chance to work on impactful projects.
- Other info: Opportunity to mentor junior statisticians and contribute to innovative initiatives.
- Why this job: Make a real difference in clinical development while utilising advanced statistical methods.
- Qualifications: Bachelor’s degree in statistics and 9+ years in clinical trials required.
The predicted salary is between 70000 - 90000 £ per year.
An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, will lead Phase I‑IV clinical studies across your region while working fully embedded within a global pharmaceutical client.
Responsibilities
- 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 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.
- Formulate an integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate processes for reducing effort and time for repeated use.
- Provide oversight of work supported by other vendors.
Qualifications
- Minimum of a 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).
Principal Biostatistician FSP - Late Phase Immunology and Neurology employer: Cytel Inc
Cytel is an exceptional employer for Principal Biostatisticians, offering a dynamic work environment fully embedded within a leading global pharmaceutical client. With a strong focus on innovation and collaboration, employees benefit from extensive professional growth opportunities, a supportive culture that values initiative and flexibility, and the chance to lead impactful clinical studies in the exciting fields of immunology and neurology.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Biostatistician FSP - Late Phase Immunology and Neurology
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