BioMarin is seeking a Medical Writer to join their team in San Rafael, CA. The role involves drafting and editing documents for clinical studies and regulatory submissions.
About the Role
As a Medical Writer, you will be responsible for preparing and managing documentation related to clinical studies, including protocols, informed consent forms, and clinical study reports. You will aid in managing study team participation, provide peer review support for regulatory documents, and ensure adherence to departmental procedures and industry standards. This position plays a crucial role in enhancing the medical writing function to meet clinical development needs and improve documentation quality.
About You
Required:
Bachelor's degree or higher in a scientific field or equivalent experience in medical or technical writing.
Up to 2 years of experience as a medical writer in the pharmaceutical industry or at least 5 years of medical or scientific writing experience.
Preferred:
Experience writing, reviewing, or editing clinical study reports and protocols.
Certification from the American Medical Writers Association or relevant training through the Drug Information Association.
Benefits
Opportunity to work in a leading biotechnology company focused on innovative science.
Collaborative work environment with cross-functional teams.
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