Senior Medical Writer - Ireland home based
As a Senior Medical Writer you will be dedicated to one of our global pharmaceutical clients; a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing lifeimproving drugs to market. We are also reviwing freelance regulatory medical writers based in Ireland. Please note , this is role is open for Ireland location only. The role and involves working on clinical trial documents for Phase 1 and Phase 2 studies Writing scope: Study protocols and protocol amendments Initial Investigator\'s Brochure (IB) and IB updates Clinical study reports Responsibilities: Plan, write, review, and coordinate the development of regulatory clinical trial documents. Ensure and coordinate quality checks for accuracy, collate reviewer’s comments, adjust content of documents as required based on internal/external input, and prepare final versions. Ensure final documents and supporting quality check documentation (with all signatures where appropriate) are placed in the appropriate document management system. #LI-NR1 #LI-Remote Key experience and requirements: Bachelor’s Degree 2-3 years of prior experience writing regulatory or clinical trial documents - Protocols/Protocol amendments/IBs Demonstrated mastery of written and verbal English Demonstrated project management and time management skills High-level end-user computer skills (e.g., word processing, tables, and graphics) Ability to work well across cultures and time zones #J-18808-Ljbffr Salary: GBP 36000 - 60000 per year Experience: 5 years required
