Senior Medical Writer

This is a fully remote position, open to applicants in United Kingdom, +7 more countries.

📋 Description

• Create and evaluate study documents such as Protocols, Synopses, Informed Consents, Data Collection Documents, and Study Reports.

• Generate scientific communications including abstracts, posters, and manuscripts.

• Conduct quality control for medical writing outputs.

• Analyze statistical results and seek input from statisticians for study reports, abstracts, manuscripts, and other related documents.

• Engage in enhancing the quality assurance system.

• Take part in bid-defense presentations to represent medical writing efforts.

• Collaborate closely with the ICON team and client account team to ensure the timely delivery of high-quality and scientifically/medically accurate projects.

⛳️ Requirements

• Possess an advanced degree in a scientific field, ideally a PhD, PharmD, or MD.

• Have over 5 years of professional experience in Medical Writing within a pharmaceutical, biotechnology, CRO, or other healthcare environment.

• Demonstrate a solid understanding of ICH/GCP and GPP guidelines or other relevant industry standards.

• Exhibit exceptional written and verbal communication skills.

• Show proficiency in computer skills.

• Ability to work efficiently and collaboratively with cross-functional teams.

• Hold the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Comprehensive health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career progression pathways.