Quantum Solutions India DLF Building
Tower D, 3rd Floor,
Chandigarh Technology Park Chandigarh 160101
Bio-Statistician 2 Opening(s)
Experience: 0 - 5 Years
Compensation: Best in the industry
Education: UG - B.Sc - StatisticsPG - M.Sc - Statistics
Desired Candidate Profile
• Experience in conducting statistical analyses of clinical data and preparation of regulatory submissions.
• Masters’ Degree (PhD, MS) in bioinformatics, biostatistics, statistics, or statistical genetics and a minimum of five years of postgraduate, professional experience.
• Ability to work independently and as a team member
• Experience using SAS/BASE and SAS/STAT in a biomedical or other health related field.
• Thorough understanding of clinical trial design, statistics and regulatory processes is desired.
• Experience in SAS/MACRO and good understanding of data management principles, such as joining data sets, indexing and record selection is desirable.
• Excellent verbal and written communication skills are required. • Experience with experimental design, linear modeling (non-linear modeling is desirable), multivariate methods and SAS pregramming as demonstrated by the completion of appropriate graduate level courses and priject work.
• Strong written and oral communication skills are required
• Masters’ Degree (PhD, MS) in bioinformatics, biostatistics, statistics, or statistical genetics and a minimum of five years of postgraduate, professional experience.
• Ability to work independently and as a team member
• Experience using SAS/BASE and SAS/STAT in a biomedical or other health related field.
• Thorough understanding of clinical trial design, statistics and regulatory processes is desired.
• Experience in SAS/MACRO and good understanding of data management principles, such as joining data sets, indexing and record selection is desirable.
• Excellent verbal and written communication skills are required. • Experience with experimental design, linear modeling (non-linear modeling is desirable), multivariate methods and SAS pregramming as demonstrated by the completion of appropriate graduate level courses and priject work.
• Strong written and oral communication skills are required
Job Description
• Prepare analysis plans and write detailed specifications for analysis files, consistency checks, tables, and figures.
• Review clinical protocols and case report forms (CRFs).
• Responsible for sample size computation as appropriate.
• Perform statistical analysis utilizing SAS and other statistical software packages.
• Interpret analysis and writes statistical sections of study reports.
• Collaborate closely with other statisticians and programmers
• Prepare and review regulatory authority statistical responses
• Review clinical protocols and case report forms (CRFs).
• Responsible for sample size computation as appropriate.
• Perform statistical analysis utilizing SAS and other statistical software packages.
• Interpret analysis and writes statistical sections of study reports.
• Collaborate closely with other statisticians and programmers
• Prepare and review regulatory authority statistical responses
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