Hybrid Medical Writer — London (Clinical Documentation)

BioMarin Pharmaceutical Inc.; United Kingdom; Hybrid; GBP 35,000 - 55,000; Full time

Job summary

A leading biotechnology company in the UK is seeking a Medical Writer to draft and edit clinical documents for regulatory submissions. This hybrid role requires strong technical writing skills and collaboration with various teams. Ideal candidates will have a Bachelor's degree or higher with experience in the pharmaceutical industry. Strong communication and project management skills are essential. The position offers a competitive salary and benefits.

Benefits

Competitive salary

Comprehensive benefits

Hybrid work model

Qualifications

• Experience as a medical writer in the pharmaceutical industry preferred.
• Ability to write high-quality documents that meet corporate goals.
• Familiarity with drug development processes and regulatory requirements.

Responsibilities

• Draft and edit documents for clinical studies and regulatory submissions.
• Manage timelines and assist in document review processes.
• Collaborate with cross-functional teams to ensure quality documentation.

Skills

Technical writing skills

Communication skills

Project management

Knowledge of biostatistics

Education

Bachelor’s degree or higher

Medical or technical writing course

Tools

Microsoft Word

Excel

Adobe Acrobat

PowerPoint

Job description

A leading biotechnology company in the UK is seeking a Medical Writer to draft and edit clinical documents for regulatory submissions. This hybrid role requires strong technical writing skills and collaboration with various teams. Ideal candidates will have a Bachelor's degree or higher with experience in the pharmaceutical industry. Strong communication and project management skills are essential. The position offers a competitive salary and benefits.