Statistical Programmer 2
24 hours ago
**Immediate Joiner Only**
Role & responsibilities
- Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials.
- Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
- Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.
- Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
- Mentoring junior programmers and assisting in training team members on programming techniques and best practices
Preferred candidate profile
- 5+ years of end-to-end statistical programming experience with SDTM, ADAM & TLF
- Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming.
- Proficiency in programming languages such as SAS, R, or Python, with experience in clinical data management systems.
- Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.
- Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.
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