Senior Statistical Programmer
4 weeks ago
At Precision Medicine Group, we are seeking a highly skilled Principal Statistical Programmer to join our team. As a key member of our Biostatistics and Data Management department, you will be responsible for performing all SAS programming tasks required for clinical trial analysis and reporting.
Key Responsibilities:
- Collaborate with functional management across the department on project deliverables and timelines.
- Maintain a positive approach and build a motivating and professional team environment.
- Develop and validate SAS programs for statistical analysis of study data.
- Create and validate randomization lists.
- Contribute to the development and maintenance of department-level SAS macros and utilities.
- Stay informed of new developments in programming relevant to the industry and contribute to innovation of new reporting systems.
- Provide guidance to the programming team on data procedures and technical standards.
- Prepare and perform internal and external training on statistical programming processes and techniques.
- Advising other employees and clients on programming techniques and principles.
- Lead internal projects to improve department processes.
- Communicate effectively with internal and external project teams.
- Support budget proposal development and reporting issues to project managers and department directors.
- Comply with all applicable regulatory requirements, company standards, and procedures.
- Participate in the development of and ensure compliance of SOPs, policies, and guidelines.
- Represent the statistical programming department during internal and external audits.
Requirements:
- Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a life science.
- At least eight years of experience as a SAS programmer for all clinical trial phases.
- Project management skills within the SAS programming functions.
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