
Programmer Developer
1 week ago
Senior Statistical Programmer
">Job DescriptionThe primary role of the Senior Statistical Programmer is to develop end-to-end statistical programming solutions for clinical trials. This includes generating summary tables, listings, graphs, and derived datasets according to SAP specifications.
Key Responsibilities:
- Develop custom programming code using SAS or other software to generate summary tables, listings, graphs, and derived datasets.
- Ensure outputs meet quality standards and project requirements.
- Perform validation programming and collaborate with other programmers and biostatisticians to resolve discrepancies.
- Maintain organized project documentation, testing, and verification/quality control programs.
- Manage multiple projects and set priorities according to project timelines.
Responsibilities (continued):
- Develop specifications for datasets and outputs of varying complexity according to statistical and sponsor requirements.
- Anticipate and address potential programming issues to establish efficient programming practices.
- Prepare and contribute in internal meetings, sponsor meetings, kickoff meetings, and bid defense meetings.
- Act as lead statistical programmer, directing programming activities of other personnel and monitoring progress on deliverables.
- Review project documentation such as SAPs, mock shells, programming specifications, annotated CRFs, and SAS database designs.
- Provide feedback to project team members to reduce inefficiencies and improve programming quality.
- Mentor programming personnel, develop training materials, and guide new associates in programming processes.
- Transfer deliverables and perform other work-related duties as assigned.
To succeed in this role, candidates should have:
- 5+ years of experience in Clinical Statistical Programming.
- Expertise in end-to-end programming, including SDTM, ADaM, and TLFs.
- Undergraduate degree in a scientific or statistical discipline, or equivalent combination of education and demonstrated programming experience.
- Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
- Excellent written and verbal communication skills; ability to read, write, speak, and understand English.
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