Senior Medical Writer

Senior Medical WriterICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.This is a hands-on scientific writing position within ICON's Global Medical Communications Group. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.What You Will Do: You will take ownership of medical writing deliverables, applying your expertise to complex challenges.Responsibilities include:Develop high-quality medical publications and communications from initial concept through final delivery.Interpret complex clinical and scientific data and translate findings into accurate, clear, and concise content.Ensure deliverables comply with applicable authorship guidelines, journal requirements, client confidentiality standards, and industry regulations.Represent assigned projects during internal and client meetings, including status updates, author discussions, and publication committee meetings.Contribute to client publication and communication plans by supporting timelines, venue selection, and alignment with drug development objectives.Support medical writing resource management, including monitoring workloads and helping coordinate junior writers.Collaborate with scientific and account management teams to meet timelines, communicate project status, and proactively identify risks or resource constraints.Assist with onboarding and mentoring new and junior medical writers.Devote approximately 5% of time to business development by providing research and writing support for proposals and organic account growth opportunities.Your Profile: You will have a strong foundation in medical writing, with the experience to work independently and guide others. Required qualifications and experience:A PhD, PharmD, or MD in a scientific or healthcare related discipline3 + years of medical writing experience (experience of high-level content development)Prior relevant experience in a medical publications/medical communications agency strongly preferredProficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skillsProven history of relevant high-level writing support, including: proficiency with ICMJE and GPP guidelines; ability to read, analyze, and interpret scientific and technical journal content; ability to develop and write to prescribed styles and formatsStrong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process.Ability to work with cross-functional teams (e.g., editorial/library services, graphics/digital services, presentations support, etc)Proficiency with commonly used software including but not limited to word processing (e.g., MS Word), graphics (e.g., PowerPoint or Prism), and bibliographic software (e.g., EndNote), and adaptability to other applicable software as may be required from time to timeExperience in resource organizing and mentoringEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.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 incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.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.