Senior Statistical Programmer

Company: NJS Associates Company
Location: Bridgewater
Posted on: August 5, 2022

Job Description:

Responsibilities

The Senior SAS Programmer works independently lead SAS programmer team interacting with the sponsor contacts. The person will be recognized internally and externally as a go-to person managing timelines, budget and deliverables priorities on behalf of the CRO.
Working experience in oncology trials including study design, RECIST data quality check, data quality check related to PFS and OS.
Excellent SAS programming skills is required.
Excellent communication skill is required.
Managing/forecasting workload with the ability to prioritize work to support multiple trials
Review of case report forms, annotated case report forms and database documentation to ensure that SAS datasets will be consistent with trial design
Generate study randomization plans and schedules
Set up tasks for SAS programming team, evaluate the timeline, priority and resources
Perform Ad-Hoc Requests and set up the chart for all ad-hoc requests to optimize the work flow, accuracy and efficiency
Write SAS programs for statistical analyses, summary tables, figures and listings.
Interact with members of the Clinical Development Team to ensure a high level of client satisfaction through the successful execution of projects
Participate in departmental infrastructure building; experience developing and implementing programing standards/best practices, developing and maintaining SAS macro and program libraries.

Qualifications

Good analytical skills and project management skills
Professional attitude and Attention to detail
Thorough understanding of statistical issues in clinical trials
Ability to clearly describe advanced statistical techniques and interpret results
Familiarity with regulatory/research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines)
Excellent skill in SAS programming require
Ability to work independently and Good mentoring/leadership skills
Good business awareness/ business development
Working Experience with CDISC is required
MS in Statistics or related discipline with more than 4 years industry experience
Industry experience; Biopharmaceutical or CRO

Keywords: NJS Associates Company, Trenton , Senior Statistical Programmer, IT / Software / Systems , Bridgewater, New Jersey