Senior Clinical Medical Writer — Lead Regulatory Documentation

BioMarin Pharmaceutical Inc.; United Kingdom; On-site; GBP 70,000 - 90,000; Full time

Job summary

A leading biotechnology firm in the United Kingdom is seeking a Principal Clinical Medical Writer to oversee medical writing staff and manage documentation for clinical development programs. The ideal candidate will have at least 8 years of experience in medical writing within the pharmaceutical industry and possess strong project management and communication skills. This role offers the opportunity to work on leading-edge treatments for genetic diseases in a collaborative environment.

Benefits

Competitive salary

Health insurance

Professional development opportunities

Qualifications

• Minimum 8 years of experience as a medical writer in the pharmaceutical industry.
• Experience writing regulatory documents such as INDs, BLAs, and clinical study reports.
• Demonstrated leadership abilities and project management skills.

Responsibilities

• Oversee medical writing staff and timelines for clinical development projects.
• Draft and edit clinical study related documents and regulatory submissions.
• Manage study team participation in document preparation and reviews.

Skills

Expertise in medical writing

Project management skills

Strong communication skills

Education

Masters (MS) or higher degree preferred

At least 8 years of experience in the pharmaceutical industry

Tools

Microsoft Word

Adobe Acrobat

Document management software

Job description

A leading biotechnology firm in the United Kingdom is seeking a Principal Clinical Medical Writer to oversee medical writing staff and manage documentation for clinical development programs. The ideal candidate will have at least 8 years of experience in medical writing within the pharmaceutical industry and possess strong project management and communication skills. This role offers the opportunity to work on leading-edge treatments for genetic diseases in a collaborative environment.