Senior Medical Writer – Early Development Services

Role Overview

• Serve as primary author for routine documents like clinical study reports and study protocols.
• Summarize data from clinical studies.
• Assist with more complex clinical and scientific documents.
• Ensure compliance with quality processes and requirements.
• Assist in program management activities, including timelines, budgets, and forecasts.
• Represent the department at project launch and review meetings.

Requirements

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred.
• Regulatory writing experience providing knowledge, skills, and abilities to perform the role (comparable to 5+ years).
• Experience working in the pharmaceutical/CRO industry required.
• Experience in managing and directing complex medical writing projects required.
• Early phase experience is preferred.

Benefits

• award-winning learning and development programme
• competitive salary
• extensive benefits package based on health and well-being of employees
• flexible working culture
• work-life balance