engineering
Posted May 4Statistical Programmer II/III (Permanent role)
at ClinChoice
United StatesOn-site
Responsibilities
- Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs)
- Perform data manipulation, analysis, and visualization using R/SAS and relevant packages
- Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables
- Ensure compliance with regulatory standards and company SOPs
- Conduct quality control (QC) and validation of programming outputs
- Support submission activities and documentation as required
Requirements
- experience in developing, validating, and maintaining statistical outputs using R, along with a solid understanding of clinical data standards. Key Responsibilities:
- Required Skills &
- Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field 3+ years of
- experience in statistical programming within the pharmaceutical/biotech industry Hands-on
- experience with R programming in a clinical trial environment
- Good understanding of R packages.
- Good understanding of CDISC standards (SDTM, ADaM)
- Strong knowledge of clinical trial data and regulatory requirements Preferred
- Experience working in an FSP model or with global pharmaceutical clients
- Familiarity with SAS alongside R is a plus
- Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the
Additional details
- Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...
- ClinChoice is currently recruiting for a Statistical Programmer II/III to join our team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment.
- Strong problem-solving and communication skills