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Sr./Principal Statistical Programmer - Remote

Posted 2 days ago
Data Analysis
Full Time
USA

Overview

The Principal Statistical Programmer works independently with minimal supervision, providing expert technical support and leadership in clinical trial data analysis and reporting.

In Short

  • Provides technical and project management leadership in SAS for clinical trial data.
  • Creates, reviews, and approves documentation for data analysis and reporting.
  • Ensures compliance with company SOPs and regulatory standards.
  • Conducts briefings and participates in technical meetings with various stakeholders.
  • Performs quality control checks on SAS code and datasets.
  • Maintains study documents and programs global utility tools.
  • Requires expertise in SAS language and clinical trial reporting.
  • Excellent communication and presentation skills are essential.
  • 8+ years of experience in the pharmaceutical industry required.
  • MS or BS in biostatistics or related field is necessary.

Requirements

  • Experience with regulatory submissions (BLAs, MAAs) is a plus.
  • Proven expertise in SAS and its procedures.
  • Strong written and oral communication skills.
  • Ability to influence across multiple functions.
  • 8+ years of experience with an MS or 10+ years with a BS in biostatistics or related field.

Benefits

  • Equal opportunity employer with a diverse environment.
  • Consideration for all applicants without discrimination.

B.B

bluebird bio

bluebird bio is a pioneering biotechnology company dedicated to developing curative gene therapies aimed at transforming the lives of patients and their families. The company fosters a collaborative and inclusive environment, where every team member's role is meaningful and respected. With a strong commitment to values such as persistence, compassion, humility, and celebration of achievements, bluebird bio emphasizes the importance of diversity in driving innovation. The organization is focused on creating a workplace that empowers individuals to act courageously and dream boldly, while ensuring compliance with regulatory standards in the biotech and life sciences sectors.

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