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Senior Statistician

3.00 to 7.00 Years   Ludhiana, Punjab   08 Jul, 2025
INSTRuCT Network
Job LocationLudhiana, Punjab
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaNot Mentioned
EmploymentTypeFull-time

Job Description

    The Clinical Project Statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with medical colleagues.The Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analysing data for these types of studies.Key Responsibilities Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study. Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created. Provides statistical support for clinical studies, including study design, sample size calculations, patient randomization, preparing annual reports, statistical analysis, interpretation of data, and reporting of results. 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. Understands and uses relevant computer languages and software packages (e.g. SAS, SPSS, R etc) Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected. Participate in peer-review work products from other statistical colleagues. Communication of Results and Inferences Collaborate with team members to write reports and communicate results. Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings. Understand disease states in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.Minimum Qualification RequirementsM.S. degree in statistics, biostatistics, or related discipline with a minimum of 3 years of experience in the Pharmaceutical/ CRO industry,Proficient in the SAS programming language,

Keyskills :
Statistical AnalysisProtocol DesignData AnalysisSAS Programming

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