Senior Clinical Editor - Fsp (permanent Home Based)

IQVIA UK

London, United Kingdom
On-site
Quality control of clinical trial documents
Subject-matter expert in medical writing
Develop quality tools and standards
Performs quality control and editing of Medical Writing deliverables to ensure accuracy, consistency, and compliance

Job Summary

  • Performs quality control and editing of Medical Writing deliverables to ensure accuracy, consistency, and compliance.
  • Provides leadership, training, and guidance to staff, and assists in resource management.
  • Takes a leading role in proposing, developing, evaluating, and implementing process changes and tools.

Matching Summary

Performs quality control and editing of Medical Writing deliverables to ensure accuracy, consistency, and compliance.

Skills & Requirements

Must-have

  • Quality control of clinical trial documents
  • Subject-matter expert in medical writing
  • Develop quality tools and standards
  • Provide training and guidance to staff
  • Manage workload and ensure on-time delivery

Nice-to-have

  • Leadership in process improvement
  • Customer liaison on QC issues
  • Familiarity with drug development trends

Key Requirements

  • Bachelor's Degree in Life sciences
  • At least 4 years' experience with clinical trial documentation
  • Significant experience in quality control review
  • Experience defining and refining processes
  • Experience training and developing others

Work Rights

Not specified

Tailored Resume

Cover Letter