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Clinical Editor (Medical/Regulatory Writing)

Gent, Flemish Brabant Province Gent

Posted: 11/07/2025 Employment Type: Contract Job Category: Medical Writing Job Number: 622780 Is job remote?: Yes Country: United Kingdom

Job Description

Are you a detail-oriented healthcare professional with a passion for precision and clarity in medical documentation? We’re seeking a talented Clinical Editor to join one of our most dynamic clients and play a pivotal role in the quality and integrity of clinical and regulatory content. This exclusive opportunity is ideal for someone eager to bring their medical background, meticulous editing skills, and proactive mindset to a global leader in medical communications.

What You’ll Do:
As a Clinical Editor, you will be at the forefront of ensuring the accuracy, consistency, and compliance of clinical documents. Your expertise will help streamline complex data into clear, polished narratives that meet the highest standards of style and factual accuracy. You’ll perform detailed fact-checks, edit for clarity and style, and collaborate with medical writers to prepare documents for inspection-readiness and regulatory review. Your keen attention to detail will ensure our content maintains excellence from draft to final submission.

Key Skills & Qualifications:
  • Native/fluent English speaker with impeccable grammar, spelling, and style skills.
  • Proven experience in quality control editing of clinical or regulatory documents.
  • Strong familiarity with AMA Manual of Style or similar style guides relevant for clinical and regulatory writing.
  • Exceptional attention to detail and a proactive approach to quality assurance.
  • Ability to fact-check complex data, verify statements, and ensure overall document integrity.
  • Excellent communication skills for effective team collaboration.
  • Experience with formatting, troubleshooting document templates, and verifying document consistency.
  • Prior experience in a QC or editing role responsible for global clinical or regulatory documentation in English.
  • Demonstrated ability to manage multiple documents, meet deadlines, and prioritize effectively.

Nice to Have Skills:
  • Lifescience, Nursing, healthcare, or medical background.
  • Previous experience working with regulatory submissions or in a clinical research environment.
  • Familiarity with document management systems or publishing tools.

This is your chance to contribute to impactful to advances in clinical research in a role that values precision and expertise. If you are ready to bring your skills to a fast-paced, globally recognized organization, we encourage you to apply now and take the next step in your professional journey!
 
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