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SENIOR PROGRAMMER LOCATION: WARRENVILLE, IL
Scope of the Job:
This new position is located at US company headquarters in Warrenville, IL. You will assist team members, including data management, clinical, medical writing, and other programmers and statisticians in the analysis of clinical trials being conducted by the company. This job requires SAS programming, good communication skills, and excellent attention to detail.
Responsibilities Include:
You will serve as the lead statistician on project teams for the execution of clinical trials.
Applies SAS programming knowledge to clinical trial data.
Extracts SAS datasets from Oracle Clinical.
Creates data management review listings.
Performs QC of tables, listings, graphs, and derived datasets.
Can independently develop computer programs to generate safety and efficacy tables, listings, graphs, and derived datasets using SAS as outlined by the statistical analysis plan.
Provide input on database design for optimal structures for the support of data collection as well as analysis.
Ability to interact with clients.
Mentors other and new programmers.
Adheres to all study/project timelines.
Documents work so other statisticians and programmers can check or modify work.
Adheres to all CliniRx policies, procedures, SOPs, and training plans.
Leads and/or contributes to internal process improvement initiatives.
Files study documents into Biometrics internal files.
Reviews draft protocols and CRFs for potential data collection and representation, or database structure problems.
Provides feedback to the project team, when requested.Other duties as assigned.
Candidate Profile and Requirements:
We seek a statistician with a minimum of 5 years of experience within the pharmaceutical industry and experience programming with SAS for statistical analysis.
We seek a professional with a Master's Degree or PhD in statistics, biostatistics, or a closely related field.
Candidates should have a sound understanding of Good Statistical Practices and various regulatory requirements (FDA, EU, ICH), knowledge of clinical trial design, FDA regulations, and quality standards.
Send Resume and Cover Letter to:
Tracy Wolfe
Phone: 512 327-7277