
Leading Statistical Programmer in Clinical Trials
13 hours ago
This is an exciting opportunity to join our team as a Senior Statistical Programmer, responsible for end-to-end statistical programming in clinical trials. The ideal candidate will have expertise in SDTM, ADaM, and TLFs, with a strong background in SAS or other required software.
The role involves collaborating with biostatisticians, sponsors, and project teams to ensure high-quality programming outputs, compliance with regulatory guidelines, and efficient project delivery. Key responsibilities include:
- Developing custom programming code using SAS or other software to generate summary tables, listings, graphs, and derived datasets according to SAP and programming specifications.
- Evaluating the quality of outputs against project requirements and regulatory standards.
- Maintaining organized, complete, and up-to-date project documentation, testing, and verification/quality control programs.
- Managing multiple projects, setting priorities, and adapting daily workload according to project timelines.
Qualifications include 5+ years of experience in Clinical Statistical Programming, with expertise in end-to-end programming, including SDTM, ADaM, and TLFs. An undergraduate degree in a scientific or statistical discipline, or equivalent combination of education and demonstrated programming experience, is also required.
In this role, you will be part of a collaborative team, working closely with biostatisticians, sponsors, and project teams to deliver high-quality results. If you are passionate about statistical programming and have a strong desire to make a difference, we encourage you to apply for this exciting opportunity.
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