Regulatory Writer

At Vivify Talent, we are seeking an experienced Regulatory Writer - Clinical Documents Specialist to join our team. As a key member of our team, you will be responsible for creating high-quality clinical documents that meet industry standards.

This role involves synthesizing complex scientific data into clear, concise documents, including clinical study reports, protocols, regulatory submissions, and marketing authorization applications. You will work closely with cross-functional teams and clients to ensure successful project outcomes.

In exchange for your expertise, you will enjoy a competitive salary of £60,000 - £80,000 per year, depending on experience. Our fully remote work setup offers flexibility and autonomy, while our focus on work-life balance means you can pursue your passions outside of work.

We require a bachelor's degree in a relevant field and proven experience in regulatory writing. If you have a passion for science and writing, and a desire to make a difference in your career, apply now