Description
As a Technical Quality Expert at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
You will be responsible for ensuring the accuracy, clarity, and quality of scientific documents and publications related to clinical trials.
Key responsibilities include:
- Editing and proofreading scientific documents, including clinical study reports and regulatory submissions
- Collaborating with medical writers to improve the clarity and effectiveness of scientific content
- Ensuring compliance with regulatory requirements and guidelines
- Providing mentorship and training to junior editors and medical writers
- Conducting thorough fact-checking and verification of data
- Staying updated with industry trends and regulatory changes
Requirements:
- Bachelor's degree in a relevant scientific discipline or communications-related field
- Extensive experience in medical editing, with a strong understanding of clinical research and regulatory documentation
- Exceptional editing and proofreading skills, with a keen eye for detail
- Strong knowledge of medical terminology and scientific writing conventions
- Excellent communication and interpersonal skills
- Proficiency in editing software and tools, as well as document management systems
ICON offers a competitive and comprehensive total rewards package, including:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities