ICON Clinical Research RMZ Millennia Business Park, Building 3A, 2nd Floor, 143 Dr. M G R Road
Kandhanchavady Chennai 600 096
Biostatistician
Experience: 1 - 3 Years
Location: Chennai, Trivandrum
Education:
UG - Any Graduate - Any Specialization PG - Post Graduation Not Required
Role: Bio-Statistician
Desired Candidate Profile
The desired candidate, under the supervision of senior biostatisticians, will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include case report form development, statistical analysis and interpretation of data, and reporting of results.
Job Description
Role Responsibility
Under the supervision of senior biostatisticians, this position is responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include case report form development, statistical analysis and interpretation of data, and reporting of results.
In addition, your tasks will include:
• Assists senior biostatisticians in providing statistical support for clinical studies, including study design, sample size calculations, patient randomization, statistical analyses, interpretation of data, and reporting of results.
• Assists senior biostatisticians in statistical aspects of case report form design.
• Assists senior biostatisticians in writing statistical analysis plans, including the definition of derived data sets, and the design of statistical tables, figures, and data listings for clinical summary reports.
• Carries out project related work in accordance with ICON standard operating procedures (SOPs) and study specific procedures (SSPs).
• Writes data quality control specifications for projects as needed.
• Understands and uses relevant computer languages and software packages. Writes programs to select, retrieve, manipulate, edit, and analyze data.
• Monitors and verifies statistical analysis programs written by statistical programmers.
• Conducts statistical analyses and interprets results of these analyses.
• Prepares statistical summary reports under the supervision of senior biostatisticians.
• Writes the statistical methods sections of integrated study reports. Reviews draft integrated study reports.
• Documents and archives analysis and programming work to ensure a complete audit trail. Participates in the setting of project document standards.
Experience and Qualification
• M.S. degree in statistics, biostatistics, or related field.
• Excellent verbal and written communication skills are required.
• Knowledge in applied parametric and nonparametric statistics and strong SAS programming skills are a must.
• Should be able to translate clients’ needs into statistical practice and educate clients in the use of statistics.
You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
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