Parsippany, New jersey
Principal SAS Programmer Job Opening in Parsippany, New jersey - Job Description
Department: Biostatistics
Position Title: Principal SAS Programmer
Reports to: Manager, SAS Programming
Location: New Jersey
Job Summary:
Provide statistical programming support to clinical trials. Produce statistical analyses, including analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastructure for project files of SAS datasets and SAS code. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.
Primary Responsibilities:
Perform or oversee team in performing all SAS programming required for clinical trial analysis and reporting on large scale projects of high complexity.
Provide statistical programming expertise for project teams.
Review the Statistical Analysis Plan in preparation for programming the planned analyses.
Lead design/development of SAS macros and other utilities to expedite SAS programming activities.
Organize and conduct internal training sessions and author papers for conferences.
Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request.
Participate in statistical program validation and quality control activities.
Develop SDTM mapping documents, ADaM Specifications; complete programming and validation of CDISC SDTM and ADaM datasets.
Review ADaM specification documents and ensure the specifications meet the analysis criteria specified in the SAP
Identify study priorities and communicate effectively with project team and management.
Ensure quality, proper documentation and meet or exceed timely completion of the project within budgeted hours.
Actively participate in study team meetings.
Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects.
Participate in review process of study documents such as the CRF, edit check specifications, and database design specifications written by Data Management.
Program data cleaning checks, as necessary, to assist Data Management's data cleaning activities.
Participate in of statistical software packages throughout the software development lifecycle.
Develop and maintain the infrastructure for project files of SAS datasets and SAS code.
Mentor junior level statistical programmers.
Desired Skills and Experiences:
5+ years experience or equivalent experience in the Clinical Industry
Strong analytical skills, with the ability to process scientific and medical data.
Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, SAS Macros and SAS/Graph.
Able to work independently.
Excellent knowledge of statistical programming.
Proficient in manipulating and analyzing SAS data.
Ability to identify data issues, present problems, and implement solutions quickly.
Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues.
Contact Below :
APPLY by sending an email or resume and one of our recruiters will reach out to you shortly.
Job Type: Full-time
Required education:
Bachelor's
Required experience:
Clinical SAS Programming: 5 years
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