Principal Stat Programmer | Hyderabad / Gurgaon
Syneos Health
India- IND-Gurgaon-Cyber-City
9d ago

Description

JOB TITLE : Senior Statistical Programmer / Statistical Programmer-II (Clinical)JOB LOCATION : Hyderabad / Pune / GurgaonPRIMARY FUNCTION : The position is responsible for performing all SAS programming tasks required to support the conduct, statistical analysis and reporting of projects, and acts as the lead statistical programmer on multiple projects.

MAJOR RESPONSIBILITIES : Act as the core project team lead to coordinate and manage all statistical programming activitiesServe as the lead programmer to design and specify the overall approach to a projects programming tasks.

Provide statistical programming liaison with the client and input for SAPs.Create and maintain programming tracking documentation.

Create, test and maintain SAS programs for clinical studies.Generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan.

Generate outputs and reports to support other departments.Perform validation on computer-generated output to verify accuracy.

Transfer of deliverables.Following departmental SOPs, OGs and relevant regulatory guidelines (e.g. ICH).EDUCATION REQUIRED : Undergraduate Degree, preferably in a scientific or statistical disciplineIn lieu of degree, either community college diploma with two (2) years of programming experience or SAS certified programmersMINIMUM TRAINING & EXPERIENCE REQUIRED : Eight (8) years experience with SAS programming in a relevant clinical trial environmentProven ability to meet deadlinesExcellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade

Qualifications

JOB TITLE : Senior Statistical Programmer / Statistical Programmer-II (Clinical)JOB LOCATION : Hyderabad / Pune / GurgaonPRIMARY FUNCTION : The position is responsible for performing all SAS programming tasks required to support the conduct, statistical analysis and reporting of projects, and acts as the lead statistical programmer on multiple projects.

MAJOR RESPONSIBILITIES : Act as the core project team lead to coordinate and manage all statistical programming activitiesServe as the lead programmer to design and specify the overall approach to a projects programming tasks.

Provide statistical programming liaison with the client and input for SAPs.Create and maintain programming tracking documentation.

Create, test and maintain SAS programs for clinical studies.Generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan.

Generate outputs and reports to support other departments.Perform validation on computer-generated output to verify accuracy.

Transfer of deliverables.Following departmental SOPs, OGs and relevant regulatory guidelines (e.g. ICH).EDUCATION REQUIRED : Undergraduate Degree, preferably in a scientific or statistical disciplineIn lieu of degree, either community college diploma with two (2) years of programming experience or SAS certified programmersMINIMUM TRAINING & EXPERIENCE REQUIRED : Eight (8) years experience with SAS programming in a relevant clinical trial environmentProven ability to meet deadlinesExcellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade

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