Senior Statistical Programmer
4 weeks ago
At Lifelancer, we're passionate about connecting talented professionals with exciting opportunities in the life sciences, pharma, and IT sectors. As a Principal Statistical Programmer, you'll play a pivotal role in delivering complex projects for a renowned pharmaceutical company.
About the RoleThis is a unique opportunity to work on innovative projects, collaborating with a global team of experts. You'll oversee studies from initial setup to completion, ensuring seamless execution and high-quality deliverables. Your expertise in statistical programming, data management, and CDISC requirements will be invaluable in driving project success.
Key Responsibilities- Plan, execute, and oversee programming activities, including resource estimation, budget management, and timeline adherence.
- Develop and maintain SDTM, ADaM, and TLF standards, ensuring compliance with CDISC requirements.
- Liaise with sponsor departments for additional programming needs, supporting publications, medical writing, and analysis.
- Ensure efficient submission activities, prioritizing quality and set-up of necessary tools and macros.
- Mentor junior team members in best practices, promoting adherence to department standards and processes.
We're looking for a seasoned professional with:
A degree in mathematics, life sciences, statistics, or computer sciences, or equivalent experience in statistical programming.At least 5 years of experience in complex clinical trials, with a solid understanding of safety and efficacy datasets and endpoints.Expert knowledge of base SAS, SAS macros, SAS/STAT, and debugging SAS programs.Broad knowledge of CDISC requirements, including define.xml, Reviewer's Guides, and submission standards.An autonomous, collaborative work style, with a keen attention to detail and a curious mind.Join our community of professionals and take the first step towards a rewarding career in statistical programming. Apply now and discover new opportunities with Lifelancer
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