Senior Medical Writer at Everest

Elevate your career with Everest Clinical Research as a Senior Medical Writer, either on-site in Markham or remotely from anywhere in Canada. This role focuses on crafting essential regulatory documents for clinical trials and marketing submissions.

As a Senior Medical Writer, you will leverage your experience to produce high-quality documentation that supports regulatory submissions and clinical study activities. You will author various key documents, ensuring adherence to company standards while meeting client needs. This position requires excellent writing skills, an understanding of clinical trials, and the ability to collaborate effectively with both internal and external stakeholders.

Key Responsibilities:

• Author regulatory documents for clinical trial applications

• Develop document templates and drafts per guidelines

• Edit medical writing products for quality and accuracy

• Manage projects liaising with sponsors and stakeholders

• Review and incorporate feedback from peer reviews

Requirements:

• Ph.D. or Master's with relevant experience

• Minimum 5 years in medical writing

• Knowledge of regulatory submission processes

• Familiarity with clinical trial documentation

• Proficient in MS Office and Adobe Acrobat

Leverage your expertise in medical writing to deliver high-quality submissions at Everest Clinical Research.
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