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970 - Senior Statistical Programmer - Ahmedabad

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Date: Feb 4, 2019

Location: Ahmedabad, GJ, IN

Company: Cytel Inc

Summary of Job Responsibilities:
 Working under the direction of Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities.
 Lead at least one study team in terms of providing technical and domain related guidance.
 May require to lead and manage a team of 2-4 members
 Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard.
 Read and understand the program specifications document.
 Prepare SAS analysis datasets, tables, listings, and figures as per specifications.
 Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery.
 Validate and transform datasets as per client assignment specifications.
 Validate tables, listings, and figures as per client assignment specifications.
 Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
 Contribute in the organization’s recruitment process by identifying need and required skill set of resources and conducting interviews to hire appropriate resources.
 Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) as applicable
Qualifications and Experience:
 B.Sc. or M.Sc. degree in Computer Science, Statistics, or related health science field with a minimum of 5 - 10 years of SAS programming experience with clinical trial data.
 Well conversant with regulatory requirements and drug development process.
 Good understanding of Clinical trial domain and good SAS programming skills
 Ability to work independently


Job Segment: Statistics, Developer, Programmer, Computer Science, Quality Manager, Data, Technology, Quality

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