Our client, a world leader in the pharmaceutical industry, is offering an excellent long-term project for a Regulatory Medical Writer. This is a fully remote contract eliminates the need for commuting, saving time and money while providing a flexible working environment. This project can also be part-time.

Benefits:

As the role is focused on writing (module 2), you will have the opportunity to leverage your expertise and even develop new skills in your area of interest

Long-term client partnerships offer financial stability and predictability for freelancers.

Responsibilities:

Crafting and compiling a range of regulatory documents such as CSRs, IBs, Protocols, Summaries, NDA/BLA/MAA, and module 2.

Collaborating effectively with colleagues to ensure the accuracy and quality of written content.

Playing a crucial role in the regulatory process to contribute to the overall success of projects.

Requirements:

Multiple years of experience in Medical Writing in the pharmaceutical industry, particularly in Clinical writing.

Proficiency in writing various regulatory documents.

Fluent level of English

If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Consulting website or on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

If you have any disability or condition that could impact your application or interview process, please share this information with us. We are committed to making any necessary adjustments to ensure a smooth and fair recruitment process for all candidates.

About NonStop: We are NonStop, a leading provider of staffing solutions across Europe and the US. Our mission is to connect talent with opportunities and support clients in finding the best talent for their teams. Visit NonStop Consulting for more information on our roles and how we can assist you further.