Senior Statistical Programmer Specializing in Clinical Data Analysis

Transform clinical research as a Senior Statistical Programmer, ensuring high standards in data analysis from a hybrid or remote setup. Your skills in statistical programming will play a crucial role in delivering quality results.
In this dynamic role, you will lead projects involving the development and validation of SDTM and ADaM datasets. Responsibilities extend to performing comprehensive QC checks, creating define.xml files, and maintaining compliance with industry standards. Engage collaboratively with cross-functional teams to support product submissions and drive success in ongoing trials.

Key Responsibilities:

• Lead statistical programming efforts and project delivery

• Develop and validate clinical trial dataset specifications

• Execute quality control processes to ensure accuracy

• Archive and document clinical trial data per SOPs

• Mentor and guide programming team members
Requirements:

• Master’s or Ph.D. in Statistics, Biostatistics, or similar

• At least four years of clinical trial programming experience

• Bachelor’s degree with a minimum of six years’ experience

• Expert knowledge of statistical software

• Strong analytical and problem-solving skills
Embrace this opportunity to enhance your career in a pivotal role that directly impacts the quality of clinical research initiatives.
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