Clinical SAS Programmer Analyst
Location
Remote
Posted by 
Kavita Madhavan on 23 Mar 2022
Job Start Date 15 April 2022
Job Type Fulltime
Sub Type W2-Salary
Payrate : Competitive rate All Inclusive
Clinical - SAS Programmer SAS CDISC SDTM Mapping SDTM ADAM TFL Tables Figures Listings (TFL) Statistical Analysis Plan (SAP)
Description
JOB TITLE: Programmer Analyst
DEPARTMENT: Biostatistics
Working within the Clinical Operations Department and Programming/Biostats functional unit,
the Programmer Analyst is responsible for building programs to create SAS datasets from the
clinical database, external data sources, and other sources while following the clinical study's
protocol or statistical plans. This position is also responsible a number of other activities related
to the creation of statistical outputs for a clinical trial.
RESPONSIBILITIES:
• Follow departmental SOPs and guidelines
• Assure Good Clinical Practices, investigator integrity, and compliance with all study
procedures.
• Ensured completeness, accuracy, and consistency of the data so that it meets the
standards of quality expected for reporting to regulatory bodies while following Good
Clinical Practices (GCP) and FDA’s validation rules for submission datasets and SDTM IG
3.2.
• Works with data management to identify issues in data quality
• Actively adapt and adjust priorities to ensure timely and quality completion of assigned
tasks
• Assist internal project team in identifying project priorities and communicating such
activities and associated timelines to departmental management
• Work independently to carry out assignments with occasional support from senior
management
• Contribute to ongoing improvement of programming processes and methodology
• Review closely CRF annotations and data specifications
• Develop programming specifications based upon the study protocol and statistical
analysis plan (SAP)
• Apply CDISC standards for SDTM and ADaM specifications when applicable
• Create persistent SAS datasets and table, figure, and listing outputs (TFLs) according to
study specifications and Statistical Analysis Plan (SAP)
• Perform validation programming for all programming deliverables
• Develop SAS macros and utility programs for repeat use across projects
REQUIREMENTS:
• Base SAS certification or the equivalent SAS programming experience, ideally in clinical
trials and/or within a CRO context.
• Ability to communicate well in written and spoken English
A commitment to working within a team and producing high quality results while
working under timeline constraints.
EDUCATION REQUIREMENTS:
• Bachelor’s degree (or higher) in Statistics, Computer Science, or other closely related
field to programming
• SAS Certification
• 2+ years SAS programming preferred
Location:
PO Box 159 Langhorne PA
19047
19047
Other Jobs
Syst Engineer --TeamDynamix Minn, MN -IT Asset Mang (ITSM/ITAM/TDX, iPaaS/Boomi (cloud based integration)
Minneapolis, Minnesota
IT - Bus Ana - ERP (JDE) - MPLS, MN (onsite, local preferred)
Minneapolis, Minnesota
Privileged Access Management (PAM) BeyondTouch Consultant - MPLS, MN (REMOTE)
Remote
IT ERP Program / Project Manager - MPLS, MN
Minneapolis, Minnesota
Info Security Sr. Project Manager - MPLS, MN (hybrid - local preferred)
Minneapolis, Minnesota