Labcorp Senior Statistical Programmer (Remote) in Helana, Montana
A Senior Statistical Programmer at Labcorp Drug Development has the opportunity to work on a variety of studies.
What you can expect:
Multiple therapeutic areas, or opportunity to specialize in early oncology
Excellent opportunities to progress and further your career
Varied, fast paced environment
Act as a Lead Statistical Programmer working with an amazing team
Home-based in the US or Canada
Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Statistical Programmer within our statistical programming department. As a Senior Statistical Programmer at Labcorp Drug Development you will assume the role of Lead Statistical Programmer for allocated studies, developing, QCing, and maintaining SAS programs to create SDTM and ADaM datasets and TFLs.
Job Primary Functions
Perform the role of the Lead Statistical Programmer:
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 as required
Develop specifications for SDTMs and ADaM datasets
Produce/QC annotated CRFs, Define XML/PDFs, Reviewers Guides and Analysis Results Metadata (ARM) to support SDTMs and ADaMs
Review SAPs and TFL shells from a programming perspective for studies
Mentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLs
Present and share knowledge at department meetings
Respond to QA and client audits, and support qualification audits
Identify processes within programming that will increase productivity, quality and efficiency
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
Typically, 3-5 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
Candidates must have experience of working as a Lead Statistical Programmer within a healthcare company
Show evidence of leading studies, experience in study set-up and review of study specific documents
Positive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environment
Good organization skills and the ability to prioritize own work
Self-motivation and ability to work independently
A cooperative and team-oriented approach
You must be fluent in English language (both verbal and written)
If you're looking for a role in a fast-paced environment leading multiple studies for key clients, then Labcorp Drug Development is the place for you!