Senior Statistical Programmer/Analyst Consultant - (remote in US)

Added
10 days ago
Type
Contract
Salary
Salary not provided

Related skills

gcp regulatory requirements clinical research clinical trial ich

📋 Description

  • Support the Programming deliveries of a clinical study or project.
  • Implement statistical programming aspects of the protocol and the clinical development program.
  • Ensure high quality is built into own deliverables and the quality delivered by other programmers.
  • Program independently with high efficiency and quality.
  • Write and/or implement specifications and oversee completeness of relevant documentation.
  • Contribute to the development of best practices to improve quality, efficiency, and effectiveness

🎯 Requirements

  • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5
  • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process
  • Good understanding of the clinical drug development process.
  • Strong communication skills and coordination skills.
  • Current knowledge of technical and regulatory requirements relevant for the role.
  • Ability to proactively manage concurrent activities within a project.
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