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sr statistical ProgrammerinVentiv Health Clinical SRE, LLC

Salary: Not Specified
Work form: Full time
Posting Date: 12/11/2025
Deadline: 02/03/2021

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Job Description :
Job Responsibilities:
Provides SAS / Statistical programming support & advice team primarily using SAS software.
Reports to local India Manager/Principal Programmer.
Works across international and functional boundaries as needed within a project team environment.
Works closely with Statistics and Data Management team members.
Review protocols, CRFs, annotated CRFs, test databases and Statistical Analysis Plans Develop, test and produce CDISC SDTM/ADAM datasets, derived datasets, tables, listings and graphs for clinical study reports. Validate team primarily using SAS software, derived datasets, tables, listings and graphs for clinical study reports. Importing and exporting data files Extraction of data from database (e.g. Clintrial) Assist with Quality Control Activities Assist with development of departmental guidelines in line with the standardization of programs and systems for the generation of CSR components Generate and maintain study documentation Attend and participate in project team meetings
Job Responsibilities:
Provides SAS / Statistical programming support & advice team primarily using SAS software.
Reports to local India Manager/Principal Programmer.
Works across international and functional boundaries as needed within a project team environment.
Works closely with Statistics and Data Management team members.
Review protocols, CRFs, annotated CRFs, test databases and Statistical Analysis Plans Develop, test and produce CDISC SDTM/ADAM datasets, derived datasets, tables, listings and graphs for clinical study reports. Validate team primarily using SAS software, derived datasets, tables, listings and graphs for clinical study reports. Importing and exporting data files Extraction of data from database (e.g. Clintrial) Assist with Quality Control Activities Assist with development of departmental guidelines in line with the standardization of programs and systems for the generation of CSR components Generate and maintain study documentation Attend and participate in project team meetings
Qualifications
Qualification:
Bachelor's degree in Statistics, Computer Science, Mathematics or related discipline. Good SAS programming skills with more than 4 years' experience in the pharmaceutical industry or a clinical research organization. Skills should include Base SAS, SAS Macro and SAS ODS. Good understanding of CDSC SDTM/ADAM standards. Basic understanding of Software Development Lifecycle. Good verbal and written communication skills. Ability to work independently on multiple projects, plan, organize and prioritize activities.
Bachelor's degree in Statistics, Computer Science, Mathematics or related discipline. Good SAS programming skills with more than 4 years' experience in the pharmaceutical industry or a clinical research organization. Skills should include Base SAS, SAS Macro and SAS ODS. Good understanding of CDSC SDTM/ADAM standards. Basic understanding of Software Development Lifecycle. Good verbal and written communication skills. Ability to work independently on multiple projects, plan, organize and prioritize activities.

Other Info

Sr Statistical Programmer
inVentiv Health Clinical SRE, LLC
Hyderabad / Secunderabad , Philippines
4-7 years
Not Specified

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inVentiv Health Clinical SRE, LLC

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inVentiv Health Clinical SRE, LLC jobs

Hyderabad / Secunderabad , Philippines


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inVentiv Health Clinical SRE, LLC jobs

Hyderabad / Secunderabad , Philippines

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