Medical Writer

Clario

Medical Writer in Global Cardiac Solutions team creating expert reports and documentation. Collaborating with scientists and stakeholders to ensure regulatory compliance and high-quality outputs.

Posted 7/28/2026full-timeRemote • 🇬🇧 United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in medical and scientific writing, with a strong focus on authoring Expert Reports and Statistical Analysis Plans while ensuring compliance with FDA, EMA, and ICH guidelines. Proven ability to manage multiple projects and collaborate effectively with cross-functional teams in the clinical research domain.

Highest-signal resume keywords

Expert Report AuthoringStatistical Analysis Plan DevelopmentClinical Trial DocumentationCardiac Safety ExperienceRegulatory Compliance Knowledge

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Scientific WritingStatistical AnalysisClinical ResearchData InterpretationDocument Quality Standards

Soft Skills

Attention to DetailOrganizational SkillsProject ManagementEffective Communication

Tools & Technologies

Microsoft Office

Industry Keywords

FDA GuidelinesEMA GuidelinesICH GuidelinesCardiologyCardiac Safety

About the role

Key responsibilities & impact

Author, edit, proofread and finalise high-quality Expert Reports based on statistical outputs, study findings and scientific conclusions.
Partner with Statistical and Scientific teams to develop and maintain Statistical Analysis Plans (SAPs) for cardiac safety studies.
Ensure all written deliverables are scientifically accurate, clearly communicated and aligned with regulatory expectations.
Collaborate with internal stakeholders to interpret study data and effectively communicate results to sponsors.
Manage document timelines and priorities across multiple studies while maintaining exceptional quality standards.
Support the preparation of additional scientific and clinical study documentation as required.
Contribute to process improvements and best practices within scientific and medical writing activities.
Participate in client interactions and scientific discussions to support successful project delivery.
Partner with Statistical and Scientific teams to support sponsors in the development of study synopses, protocols and other clinical research documents related to cardiac safety.
Coordinate the timely delivery of Expert Reports, Statistical Analysis Plans and other key study outputs.
Maintain a strong understanding of FDA, EMA, ICH and other relevant regulatory guidance related to clinical trial reporting and documentation.
Stay current with developments in clinical research, cardiac safety assessment and scientific communication.
Support cross-functional initiatives within the broader Digital Physiology business.

Requirements

What you’ll need

Bachelor's degree in Life Sciences, Clinical Research, Pharmacy, Healthcare, or a related scientific discipline
Advanced degree (MSc, PhD or PharmD) preferred
Minimum 5 years' experience in medical, scientific or clinical writing within the pharmaceutical, biotechnology, CRO or clinical research sectors
Experience authoring scientific reports, statistical analysis plans, clinical study documentation and regulatory deliverables
Previous experience supporting Cardiology, Cardiac Safety, ECG analysis, electrophysiology or cardiovascular clinical trials is required
Strong understanding of clinical trials, ICH guidelines, and FDA and EMA regulatory requirements
Proven ability to interpret and communicate complex clinical and statistical data
Excellent written communication skills, attention to detail and document quality standards
Strong organisational and project management skills, with the ability to manage multiple priorities and deadlines
Experience collaborating with cross-functional teams, including statisticians, physicians and scientific experts
Proficient in Microsoft Office applications, particularly Word.
Able to work independently and effectively within a fast-paced global environment.

Benefits

Comp & perks

Competitive compensation and incentive programmes
Private healthcare, pension and life assurance
Flexible working arrangements supporting work-life balance
Generous annual leave and wellbeing initiatives
Opportunities for professional growth within a global organisation
Access to collaborative global teams and innovative technologies
The opportunity to contribute to research that improves patient outcomes worldwide