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Clinical Statistical Programmer - Pharma (4-13 yrs)

4.00 to 13.00 Years   Bangalore   09 Sep, 2022
Recruise India Consulting Pvt Ltd
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryManagement Consulting / Strategy
Functional AreaQuality (QA-QC)Statistics / Analytics
EmploymentTypeFull-time

Job Description

    The purpose of the Clinical Statistical Analyst is to assist during the development of data analysis plans in collaboration with statistical colleagues, physicians, veterinarians, and/or medical colleagues. The Clinical Statistical Analyst is responsible for establishing are porting database and for analyzing clinical trial data by working with clinical research associates/clinical development associates and project statisticians.Key Responsibilities :- The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.Statistical Trial Analysis :- Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.- Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is created.- Collaborate with data management in the planning and implementation of data quality assurance plans.- Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.- Effectively justify methods selected and implement previously outlined analysis plans.- Conduct peer-review of work products from statistical colleagues.- Effectively utilize current technologies and available tools for conducting the clinical trial analysis.Communication of Results and Inferences :- Collaborate with other statistical colleagues to write reports and communicate results.- Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.- Assist or respond to regulatory queries working in collaboration with other statistical colleagues.Therapeutic Area and Systems Knowledge :- Understand relevant disease states in order to enhance the level of customer focus and collaboration.- Ensure replication of tools and systems, where applicable and stay informed of technology advances.Regulatory Compliance :- Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes and training,

Keyskills :
sassas programmingsdtmdata managementdata quality assurancedata qualitydata analysisquality assuranceclinical researchstatistical analysisregulatory submissionsclinical trialresearchbusinessplanninganalysis

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