At a Glance
- Tasks: Lead the creation of high-quality medical documents and collaborate with diverse teams.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
- Other info: Be part of an inclusive culture that values integrity and collaboration.
- Why this job: Make a real impact in healthcare by communicating vital scientific information.
- Qualifications: Bachelor's degree in life sciences and significant medical writing experience required.
The predicted salary is between 60000 - 80000 £ per year.
Company Overview
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Values
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Role Summary
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information.
What You Will Do
- You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations.
- Leading the preparation and review of clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity.
- Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development.
- Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards.
- Mentoring and training junior medical writers, fostering a culture of excellence and professional growth.
- Staying current with industry trends and regulatory guidelines to inform writing practices and maintain high-quality outputs.
- Acting as a lead medical writer for complex projects and leading clinical/regulatory marketing approval applications for new biologics and drugs.
Your Profile
- A bachelor's degree in life sciences, pharmacy, or a related discipline.
- Significant experience in medical writing, particularly in regulatory submissions and clinical documentation.
- Experience with Neuroscience is a big plus.
- Strong understanding of regulatory requirements and industry standards for clinical writing.
- Exceptional writing and editing skills, with a keen eye for detail and clarity.
- Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams and stakeholders.
Legal Requirements
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
- Competitive base salary and performance related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
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