Regulatory Medical Writer
Have you got experience in Regulatory Medical Writing & looking for a new and exciting opportunity? My client who is a mid-size CRO is currently looking for a Regulatory Medical Writer to join their team Fully Remotely, Anywhere in Europe on a permanent basis! My client works with some of the top companies in the world allowing you to grow your professional skills exponentially the more you work with them. Due to the growth rate of the company they have a heavy internal promotion culture (over 90%!) which means there is a concrete chance of further opportunities down the line.

Responsibilities:

• Draw up, edit and review preclinical/clinical documents
• Develop scientific manuscripts and abstracts reporting clinical study results, as well as slide & poster presentations
• Coordinate and manage documents to produce submission-ready content for customers
• Perform literature searches and reviews as necessary to obtain background information for the development of documents

Requirements:

• Master's degree in Biomedical / Scientific discipline
• At least 3 years of experience as a Medical Writer
• Excellent knowledge of ICH-GCP guidelines and methodology of clinical research
• Knowledge of medical concepts and terminologies

NonStop Consulting is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.