10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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.
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10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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 of high-quality regulatory and clinical documents âą Oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations âą Prepare and review clinical study reports, protocols, and regulatory documents for accuracy and clarity âą Collaborate with cross-functional teams to gather and synthesize information for document development âą Provide guidance on medical writing best practices and ensure adherence to regulatory requirements âą Mentor and train junior medical writers, fostering a culture of excellence and professional growth âą Stay current with industry trends and regulatory guidelines
âą A bachelor's degree in life sciences, pharmacy, or a related discipline âą Significant experience in medical writing, particularly in regulatory submissions and clinical documentation âą Experience with Neuroscience is a big plus âą Strong understanding of regulatory requirements and industry standards for clinical writing âą Exceptional writing and editing skills, with a keen eye for detail and clarity âą Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams and stakeholders
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 Nowđ May 29
Principal Medical Writer at Veristat planning and preparing regulatory documents and medical communications. Supporting product development phases and collaborating with cross-functional teams.
đŹđ§ United Kingdom â Remote
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŹđ§ UK Skilled Worker Visa Sponsor
đ April 21
Medical Writer evaluating and authoring clinical development documents for regulatory submissions. Working in a remote role within a supportive and innovative team environment.
đŹđ§ United Kingdom â Remote
đ° Private Equity Round on 2022-06
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŹđ§ UK Skilled Worker Visa Sponsor