- Provide input on protocols such as study design, sample size calculations, and patient randomization schemes.
- Handle statistical aspects of case report form design.
- Review study database structures, edit checks, and data management coding convention.
- Prepare statistical analysis plans, including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports.
- Conduct statistical analyses.
- Interpret data and report results.
- Write the statistical methods sections of integrated study reports.
- M.S. or Ph.D. degree in statistics, biostatistics, or a related field.
- Excellent verbal and written communication skills.
- Knowledge in applied parametric and nonparametric statistics and SAS programming skills.
- Ability to translate clients' needs into statistical practice and educate clients in the use of statistics.
- Experience working in oncology clinical trials is preferable but not essential.
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Senior Statistician, Oncology - London, United Kingdom - Proclinical Staffing
Description
Proclinical is seeking a dedicated Senior Statistician who is passionate about advancing and improving patients' lives. This role is integral to our mission of becoming the partner of choice in drug development. As a Senior Statistician, you will be responsible for planning, monitoring, organizing, and reviewing the activities of biostatisticians and programmers working on studies of moderate complexity. Your focus will be on ensuring that individual studies are delivered on time, on budget, and to the required quality.
Key Responsibilities
Requirements
If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.