Business Type: Clinical Research Organisation, Contract Research Organisation
Position type: Permanent
Location: United Kingdom - South East
This position is responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.
M.S. degree in statistics, biostatistics, or related field with at least 4 years of relevant experience (at least 3 of which must be in the pharmaceutical industry); or Ph.D. in statistics, biostatistics, or related field with at least 2 years of relevant experience (at least 1 of which must be in the pharmaceutical industry). In-depth knowledge of study designs, and statistical analysis conventions in one or more therapeutic areas. Excellent verbal and written communication skills are required. Knowledge in applied parametric and nonparametric statistics and strong SAS programming skills are a must. Must be able to translate clients’ needs into statistical practice and educate clients in the use of statistics.
“Hobson Prior is a corporate member of the REC and operates strictly within the regulations governing the conduct of employment businesses. This requires us to provide detailed information to candidates in relation to specific roles prior to the submission of their personal details and prohibits the disclosure of information relating to candidates without their consent.”
To apply, please reply with an up to date copy of your CV quoting reference 'grv-1700'.
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