SuperStaff

Comprehensive BPO, RPO, and Call Center Outsourcing Solutions for Growing Businesses

Principal Statistical Programmer

Software EngineerSoftware EngineerFull TimeRemoteTeam 201-500Since 2009H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

17 days ago

Salary

Not specified

Bachelor Degree5 yrs expEnglish

Job Description

• Working under the direction of the 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 required to lead and manage a team of 2-4 members • Experience of working on Oncology TA is mandatory. • 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. • Coordinate 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 needs and required skill sets of resources and conducting interviews to hire appropriate resources. • Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable

Job Requirements

  • BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data.
  • Well-conversed with regulatory requirements and drug development process.
  • Good understanding of the Clinical trial domain and good SAS programming skills
  • Ability to work independently.

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