Senior Medical Writer

Parexel is a global clinical research organization that provides clinical development and regulatory services. The Senior Medical Writer leads clinical trial transparency submissions, advises clients on disclosure requirements, and mentors junior team members.

• Lead clinical trial transparency submissions and regulatory document reviews
• Advise clients and internal teams on disclosure requirements
• Manage complex disclosure projects from initiation through delivery
• Develop process improvements and disclosure best practices
• Mentor junior team members on disclosure and regulatory compliance
• Ensure submissions meet quality standards and regulatory requirements

Education

Bachelor's degree

Degree

life sciences, health sciences

Domain

clinical research

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