Clinical SAS Programmer

Chicago, IL, US • Posted 2 days ago • Updated 58 minutes ago

Full Time

On-site

Fitment

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Job Details

Skills

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

Summary

Responsibilities:

Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
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
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
Provides programming support for adhoc analysis
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)
Manages timelines and schedules of specific phases of projects with internal personnel and external vendors
cts as lead programmer for a study
Reviews or validates statistical deliverables of vendors for assigned project(s)

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 5 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.
bility to prioritize and multi-task effectively
Demonstrated positive attitude and the ability to work well with others.

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: ddfb99db82eb0e9928b8115b07916264
Posted 2 days ago

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Clinical SAS Programmer

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Job Details

Skills

Summary

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