Statistical Programming Analyst
Job in
Fayetteville, Cumberland County, North Carolina, 28305, USA
Listed on 2026-07-13
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-13
Job specializations:
-
IT/Tech
Data Analyst, Data Security, Data Science Manager, Data Scientist
Job Description & How to Apply Below
- Co-lead (with supervision), coordinates and manages timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables of projects.
- Co-author basic CDISC ADaM (analysis data model) analysis data set specifications including the identification of potential data issues or areas of critical data examination.
- Works with statistics on defining and documenting programming endpoint algorithms across a study, drug program.
- Manage under supervision the end-to-end programming of deliverables from CRF collections through electronic submission including preparation of electronic submissions (ESUB) components (input to reviewer's guides, annotated CRF, define and XPTs); works with SMEs in SSM to ensure compliance to ESUB standards.
- Participate in efforts to remedy departmental inefficiencies in conjunction with QPT.
- Serve as the Statistical Programming co-lead to achieve milestones for a study; collaborates with PL and/or manager on issues or resource needs.
- Verify program consistency and usage of data, analysis and submission standards within a study in consultation with data standards, statistical submissions management, and the data strategy plan.
- Inform internal and external project team members of statistical programming requirements, deliverable status, and resource needs.
- Bachelor’s degree required, Masters or PhD in Statistics or Mathematics preferred
- 2+ years relevant work experience within an organization with a focus on data management and analysis
- 2+ years SAS Base programming with 5+ years using SAS STAT, GRAPH and MACRO
- 2+ years relevant industry experience
- 2+ years clinical trial experience
- 2+ years clinical database experience
- CDISC and/or submissions experience
- Some knowledge of drug development process and clinical trials
- Some knowledge of drug submission requirements, relevant ICH and FDA/EMEA/ROW guidelines
- Some familiarity with UNIX as well as software development packages (R, Imaging and Genomics software packages)
- Some familiarity AI and ML concepts
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