Senior Medical Writer – Hybrid London, Regulatory Docs

BIOMARIN; Greater London; Hybrid; GBP 50,000 - GBP 70,000; Full time

Job summary

A global biotechnology firm in London seeks a Senior Medical Writer with significant experience in medical writing, able to draft and manage clinical study documents for regulatory submissions. The role requires strong project management and collaboration skills in a hybrid work environment, with an emphasis on advanced scientific understanding and effective communication. The ideal candidate will have a Bachelor's degree, favorable certifications, and familiarity with pharmaceutical industry regulatory requirements.

Qualifications

• Minimum experience in medical writing with up to 6 years in the pharma industry.
• Experience writing protocols and clinical study reports required.
• Advanced understanding of the drug development process.

Responsibilities

• Drafts and edits clinical study documents and regulatory submissions.
• Manages document review and comment adjudication processes.
• Collaborates with cross-functional teams to meet project goals.

Skills

Medical writing

Editing documents

Project management

Cross-functional collaboration

Regulatory knowledge

Education

Bachelor’s degree in a scientific field

Certification from American Medical Writers Association

Tools

Microsoft Word

Adobe Acrobat

SharePoint

Job description

A global biotechnology firm in London seeks a Senior Medical Writer with significant experience in medical writing, able to draft and manage clinical study documents for regulatory submissions. The role requires strong project management and collaboration skills in a hybrid work environment, with an emphasis on advanced scientific understanding and effective communication. The ideal candidate will have a Bachelor's degree, favorable certifications, and familiarity with pharmaceutical industry regulatory requirements.