10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
đ„ 35 minutes ago
đ United Kingdom, France, +8 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ„đ Medical Writer
đ» Ghost score 10%
Where this job comes from
Posted on ICON plc's careers page, not through a job board
First seen by Remote Rocketship 35 minutes ago
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
âą Lead the development and execution of medical writing strategies for clinical research projects âą Deliver high quality relevant Clinical Pharmacology & Pharmacometrics documents, including population PK/PD data transfer plans, population PK/PD analysis plans, and population PK/PD reports âą Prepare CSRs, protocols, study reports, and other scientific documents âą Drive the document preparation process âą Receive and review primary statistical output âą Draft and distribute documents for review âą Incorporate and resolve comments with all reviewers âą Provide scientific and medical writing consultancy to project teams âą Adhere to client SOPs, WIs, policies, local regulatory requirements, and ICH-GCP âą Communicate clearly with clinical pharmacology and pharmacometrics leaders and other team members âą Ensure deliverables are inspection ready and compliant with relevant requirements âą Maintain central planning of population PK/PD document writing and QC deliverables
âą Advanced degree in Life Sciences, Pharmacy, Medicine, or related field âą Minimum of 3-5 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry âą Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses âą Excellent writing, editing, and proofreading skills âą Ability to communicate scientific concepts to diverse audiences âą Strong understanding of regulatory requirements, including ICH-GCP, FDA, and EMA, governing the preparation and submission of clinical documents and publications âą Experience interacting with regulatory agencies during the review and approval process âą Ability to work effectively in a fast-paced, deadline-driven environment âą Ability to manage multiple projects simultaneously and prioritize tasks based on project timelines and deliverables âą Excellent interpersonal and communication skills âą Ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes âą Legal right to work in the country where the role is based
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
đ October 19
Senior Medical Writer producing clinical and regulatory documents for Syneos Health, a life sciences services organization. Coordinating cross-functional reviews and mentoring medical writers.
đ September 30
Senior Medical Writer developing clinical regulatory documents for TransPerfectâs life-sciences clients. Leading authoring, review cycles, and cross-functional delivery across UK-based teams.
đ September 30
Senior Medical Writer preparing clinical regulatory documents for TransPerfectâs language-services business. Leading authoring, review cycles, and cross-functional delivery for drug-development programs.
đ September 29
Associate Medical Writer creating accurate scientific content for BOLDSCIENCEâs medical communications accounts. Developing publications, presentations, and digital materials across therapy areas under senior guidance.
đ September 28
Senior Medical Writer producing clinical regulatory documents for TransPerfectâs life-sciences clients. Leading authoring, review cycles, timelines, and cross-functional stakeholder coordination.