Your Responsibilities
With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff.
Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments and the client etc.
Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs and perform QC of SDTM ADaMs and TFLs.
Produce Define XML / PDFs Analysis Results Metadata (ARM) annotated eCRFs and Reviews Guides to support SDTMs and ADaMs.
With support from senior programming staff develop specifications for SDTMs and ADaM datasets.
Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff.
Respond to QA and client audits with support from senior programming staff.
And all other duties as needed or assigned.
Your Profile
Minimum Bachelors degree preferably in mathematics statistics computing life science health science or related subjects.
Typically 1 - 2 years of SAS programming experience in the CRO or Pharmaceutical industry or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
Knowledge of CDISC requirements.
Business fluency in English both spoken and written is a must.
Learn more about our EEO & Accommodations request here .
Key Skills
* Business Development
* Customer Service
* Attorney
* CISSP
* Data Analysis
Employment Type: Full-Time
Experience: years
Vacancy: 1
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