Summary Of 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.
  
  

Qualifications (Minimum Required)

• Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
• Experience and/or education plus relevant work experience, equating to a Bachelor's degree.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Language Skills Required:
• Speaking: Yes, English Required.
• Writing/Reading: Yes, English Required.
  
  

Experience (Minimum Required)

• 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.
  
  

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