Senior Medical Writer - Clinical & Regulatory Docs

BioMarin Pharmaceutical Inc.; United Kingdom; On-site; GBP 55,000 - 75,000; Full time

Job summary

A global biotechnology company is seeking a Senior Medical Writer to manage and prepare clinical study documents. This position requires advanced knowledge in medical writing and regulatory standards, a bachelor's degree in a scientific field, and at least 6 years of relevant experience. The role will involve collaboration with cross-functional teams and emphasis on clear communication and document management to ensure quality and efficiency.

Qualifications

• Experience in medical writing industry for at least 6 years.
• Advanced understanding of the drug development process.
• Capable of managing multiple documents and cross-functional teams.

Responsibilities

• Draft and edit clinical study documents.
• Manage study team participation in document preparation.
• Provide peer review and editing support for regulatory documents.

Skills

Medical writing

Technical writing

Regulatory knowledge

Project management

Communication skills

Education

Bachelor’s degree or higher in a scientific field

Tools

Microsoft Word

Excel

Adobe Acrobat

MS Project

Job description

A global biotechnology company is seeking a Senior Medical Writer to manage and prepare clinical study documents. This position requires advanced knowledge in medical writing and regulatory standards, a bachelor's degree in a scientific field, and at least 6 years of relevant experience. The role will involve collaboration with cross-functional teams and emphasis on clear communication and document management to ensure quality and efficiency.