Medical Writer - Clinical Documentation & Regulatory

biomarin; San Rafael (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

Biomarin is seeking a Medical Writer 1 in San Rafael, California. The role involves drafting and editing documents for clinical studies and regulatory submissions, as well as managing timelines and supporting document review processes.

The ideal candidate will have a Bachelor's degree or higher and experience in medical writing, with a focus on effectively communicating complex scientific concepts. This is a full-time position that aims to enhance productivity and documentation quality.

Qualifications

• Up to 2 years as a medical writer in the pharmaceutical industry.
• At least 5 years of medical or scientific writing experience.
• Familiar with the drug development process.

Responsibilities

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

Skills

Medical writing

Project management

Communication

Regulatory knowledge

Education

Bachelor’s degree or higher (scientific focus)

Medical or technical writing course(s)

Tools

Microsoft Word

Adobe Acrobat

Excel

Job description

Biomarin is seeking a Medical Writer 1 in San Rafael, California. The role involves drafting and editing documents for clinical studies and regulatory submissions, as well as managing timelines and supporting document review processes.

The ideal candidate will have a Bachelor's degree or higher and experience in medical writing, with a focus on effectively communicating complex scientific concepts. This is a full-time position that aims to enhance productivity and documentation quality.