You can be 100% home-based or if you prefer, you can work from our local office in your home country.

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 Bachelor’s 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.