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А drug development service company Covance is seeking an Associate Director to consult on innovative and adaptive clinical trial designs, provide support for DMC/DSMB data review meetings, and analyze all parts of any clinical study.
Job Primary Functions
We are seeking an Associate Director, Biostatistics to consult on innovative and adaptive clinical trial designs, provide support for DMC/DSMB data review meetings, and analyze all parts of any clinical study. The selected candidate will provide statistical input into other disciplines’ activities and participate in interdepartmental processes; provide technical solutions and advice to staff and clients on statistical processes; train less experienced biostatisticians within project activities; and be responsible for the development of Statistical Sections of Protocol including statistical methodology, statistical programming procedures, definition of derived variables, and data handling rules and data display templates.
Master’s degree, equivalent, or higher in Biostatistics or related field
Demonstrate good knowledge in supporting data monitoring committees with excellent organizational skills, communication skills and writing skills
Ability to program in one or more statistical software packages (SAS®) used to conduct statistical analyses. SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis
Ability to perform sample size determination using appropriate statistical software such as NCSS PASS, Cytel EAST, StatSols nQuery, or SAS.
Proven ability to effectively communicate statistical concepts
Interpersonal and effective communication skills; able to communicate appropriately throughout Covance and with its clients.
Excellent problem-solving skills, and a willingness to take ownership of decision-making.
A good knowledge of the overall clinical trial process and of its application within Covance Clinical Development
Competence in the preparation of Statistical Analysis Plans, analysis, reporting, etc. across a variety of trials
Specific up-to-date knowledge of statistics as applied in clinical trials for at least one therapeutic area.
Fluent in English language (both verbal and written).
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