Senior Nonclinical Writer — Remote UK (Reg Submissions)

MMS; City of Edinburgh; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization is seeking a skilled individual to develop and manage technical nonclinical documents. You will lead writing projects, collaborate with cross-functional teams, and ensure compliance with regulatory guidelines. The ideal candidate holds a BS in pharmacology or related fields and has a strong background in regulatory writing. This is a full-time remote position based in the UK.

Qualifications

• 2 years of pharmaceutical regulatory nonclinical writing experience.
• Knowledge of GLP ICH guidelines and applicable regulatory requirements.
• Hands-on experience with clinical trial and pharmaceutical development preferred.

Responsibilities

• Develop and write highly technical nonclinical documents.
• Lead projects independently with minimal oversight.
• Collaborate with cross-functional teams.

Skills

Strong writing and analytical skills

Excellent written / oral communication

Organizational expertise

Proficiency with MS Office applications

Ability to operate in negotiation and analytical environments

Education

BS in pharmacology, toxicology, biology, or chemistry

Tools

Content Management Systems

SharePoint

Veeva

Adobe Captivate

Job description

A leading clinical research organization is seeking a skilled individual to develop and manage technical nonclinical documents. You will lead writing projects, collaborate with cross-functional teams, and ensure compliance with regulatory guidelines. The ideal candidate holds a BS in pharmacology or related fields and has a strong background in regulatory writing. This is a full-time remote position based in the UK.