Senior Nonclinical Writer — Remote UK Regulatory Submissions

MMS Holdings Inc.; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization in the UK seeks a Senior Writer for a remote position focusing on developing and managing technical nonclinical documents. Candidates should possess at least 2+ years of regulatory writing experience, strong analytical skills, and proficiency in MS Office. This role involves collaboration with multi-disciplinary teams to ensure compliance with regulatory guidelines, making it ideal for proactive individuals eager to contribute to innovative clinical research projects.

Qualifications

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

Responsibilities

• Develop and write nonclinical documents for regulatory submissions.
• Lead projects with minimal oversight and ensure scientific integrity.
• Collaborate with cross-functional teams for document accuracy.

Skills

Strong writing and analytical skills

Excellent written/oral communication

Project management skills

Regulatory guidance understanding

Organizational expertise in nonclinical subject area

Education

BS + in pharmacology, toxicology, biology, or chemistry

Tools

MS Office applications

Job description

A leading clinical research organization in the UK seeks a Senior Writer for a remote position focusing on developing and managing technical nonclinical documents. Candidates should possess at least 2+ years of regulatory writing experience, strong analytical skills, and proficiency in MS Office. This role involves collaboration with multi-disciplinary teams to ensure compliance with regulatory guidelines, making it ideal for proactive individuals eager to contribute to innovative clinical research projects.