Manager, Medical Writing

Manager, Medical Writing - Imaging

• ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
• 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.
• As a Manager, Medical Writing at ICON, you will lead a team of medical writers to produce high-quality, scientifically accurate documents in support of clinical trials.
• What You Will Do: Your focus will be on coordinating medical writing delivery, resolving issues, and developing team capability.
• Key responsibilities include: Managing the medical writing team, providing guidance and oversight to ensure high-quality, consistent, and scientifically sound documentation.
• Overseeing the preparation of clinical study reports, regulatory submissions, protocols, investigator brochures, and other key clinical documents.
• Collaborating closely with cross-functional teams including clinical, regulatory, and project management teams to ensure alignment and accuracy in documentation.
• Ensuring that all documents comply with applicable regulatory guidelines and internal standards while maintaining clear and concise scientific communication.
• Tracking project timelines and deliverables, ensuring that all documentation is completed and submitted within established deadlines.
• Continuously improving writing processes and templates, incorporating best practices to enhance the efficiency and quality of the medical writing function.
• Your Profile: You will have solid medical writing experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience

• Bachelor's degree in life sciences, health sciences, or a related field is preferred, with extensive experience in medical writing within the pharmaceutical or clinical research industry.
• Proven experience in managing medical writing teams and overseeing the development of regulatory and clinical documents.
• Strong knowledge of regulatory requirements, clinical trial processes, and scientific writing best practices.
• Excellent writing, editing, and communication skills, with the ability to convey complex scientific concepts clearly and accurately.
• Strong organizational and leadership abilities, with experience in managing multiple projects and ensuring on-time delivery.
• Detail-oriented, adaptable, and proactive, with a commitment to maintaining the highest standards in medical writing.
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

• ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
• Benefits may include: 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
• Benefits may vary depending on role and location.
• Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

• 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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• Are you a current ICON Employee? Please click here to apply