Medical Writer

Overview

As a Medical Writer in the Global Cardiac Solutions team, you translate complex clinical and statistical data into clear scientific deliverables that support regulatory submissions and critical development decisions. You collaborate with statisticians, scientists and cardiac safety experts to produce expert reports, SAPs and related documentation. This role suits an experienced writer who aims to advance life-changing therapies by ensuring accuracy, regulatory alignment and compelling communication. You will work in a fast-paced, global environment with cross-functional teams to deliver high-quality outputs that impact patient outcomes.

Pay / Benefits

• Competitive compensation and incentives
• Private healthcare, pension and life assurance
• Flexible working arrangements
• Generous annual leave and wellbeing initiatives
• Opportunities for professional growth
• Access to collaborative global teams and innovative technologies

Responsibilities

• Author, edit, and finalize Expert Reports based on statistical outputs and study conclusions
• Develop and maintain Statistical Analysis Plans (SAPs) for cardiac safety studies in collaboration with Statistical and Scientific teams
• Ensure deliverables are scientifically accurate and regulatorily aligned
• Collaborate with stakeholders to interpret study data and communicate results to sponsors
• Manage document timelines across multiple studies while upholding quality
• Prepare additional scientific and clinical study documentation as needed
• Contribute to process improvements in scientific and medical writing
• Participate in client interactions and scientific discussions to support project delivery
• Support development of study synopses, protocols and other clinical research documents in cardiac safety
• Coordinate timely delivery of Expert Reports, SAPs, and other outputs
• Maintain understanding of FDA, EMA, ICH and regulatory guidance on clinical trial reporting
• Stay current with developments in clinical research and cardiac safety communication
• Support cross-functional initiatives within the Digital Physiology business

Key requirements

• Minimum 5 years’ experience in medical, scientific or clinical writing in pharma, biotech, CRO or clinical research
• Experience authoring scientific reports, SAPs, clinical study documentation and regulatory deliverables
• Cardiology, Cardiac Safety, ECG analysis, or cardiovascular trial experience required
• Strong understanding of clinical trials, ICH guidelines, and FDA/EMA requirements
• Proven ability to interpret and communicate complex clinical and statistical data
• Excellent written communication, detail orientation, and document quality standards
• Strong organisational and project management skills with ability to handle multiple priorities
• Experience collaborating with cross-functional teams including statisticians and scientists
• Proficient in Microsoft Word and other Office tools
• Ability to work independently in a fast-paced global environment

• excellent written communication
• attention to detail
• strong organisational skills
• Statistical Analysis Plans (SAPs)
• interpretation of statistical data
• clinical trial reporting

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