Senior Nonclinical Writer - Remote UK

MMS; Remote; GBP 45,000 - 60,000; Full time

Job summary

A clinical research organization based in the UK is seeking a Regulatory Writer to develop and manage technical nonclinical documents. The ideal candidate will have a BS in pharmacology or a related field and at least 2 years of experience in regulatory writing. Responsibilities include leading document development and collaborating with cross-functional teams to ensure regulatory compliance. This is a full-time remote role with an emphasis on written communication skills and a strong understanding of regulatory guidelines.

Qualifications

• 2 years of pharmaceutical regulatory nonclinical writing experience.
• Knowledge of GLP ICH guidelines and applicable regulatory requirements.
• Strong writing and analytical skills required.

Responsibilities

• Participate in the development, writing, and management of nonclinical documents.
• Lead projects independently with minimal oversight.
• Collaborate with cross-functional teams.

Skills

Content Management Systems

Technical Writing

Writing Skills

User Research

Copywriting

Education

BS in pharmacology, toxicology, biology or chemistry

Tools

MS Office applications

SharePoint

Veeva

EndNote

Job description

A clinical research organization based in the UK is seeking a Regulatory Writer to develop and manage technical nonclinical documents. The ideal candidate will have a BS in pharmacology or a related field and at least 2 years of experience in regulatory writing. Responsibilities include leading document development and collaborating with cross-functional teams to ensure regulatory compliance. This is a full-time remote role with an emphasis on written communication skills and a strong understanding of regulatory guidelines.