SAS Programmer - Katalyst Healthcares and Lifesciences - New York, NY, US | Dice.com

Katalyst Healthcares and Lifesciences

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SAS Programmer

New York, NY, US • Posted 60+ days ago • Updated 13 hours ago

Full Time

On-site

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Job Details

Skills

Quality Control
Macros
Graphical User Interface
Forms
Database
Base SAS
SAS/STAT
SAS/GRAPH
SAS/MACROS
Statistics
Computer Science
Clinical Trials
SAS
Reporting
CDISC
SDTM
Conflict Resolution
Problem Solving
Communication
Documentation
Biostatistics
Data Management
Medical Writing

Summary

Responsibilities:

Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
Provides input in the design and development of case report forms and clinical databases.
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
Programs quality checks for clinical study raw data and report the findings to Data Management
Provides input in the design and development of case report forms and clinical study databases.
Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
Provides programming support for adhoc analysis.

Requirements:

MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 4+ years.
Experience in providing statistical programming support to early and late phase clinical trials.
Excellent skills in SAS programming and statistical reporting.
Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
Familiarity with FDA and ICH regulations and guidelines.
Excellent problem-solving skills.
Good written and verbal communication skills and organizational and documentation skills.
bility to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 1c964c2a4470958e0533fd7ab2fdf482
Posted 30+ days ago

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