Lead Medical Writer Clinical Research

Position: Lead Medical Writer for Clinical Research
Step into a leadership role with Everest Clinical Research as a Senior Medical Writer. Work from home across Canada or join the team in Markham. Deliver critical documentation for clinical trials and regulatory approvals.

In the position of Senior Medical Writer, you will be responsible for authoring a range of pivotal regulatory documents, including clinical study protocols, investigator brochures, and integrated summaries. This multifaceted role demands collaborative skills and the ability to provide clear, effective communication while managing the writing life cycle from initiation to submission.

Key Responsibilities:

• Author key regulatory submissions for drug trials

• Develop document shells in line with required styles

• Edit and finalize documents based on reviewer feedback

• Manage timelines and quality control for projects

• Conduct peer reviews and enhance team capabilities

Requirements:

• Ph.D. in a related field or extensive experience

• Minimum 5 years in clinical writing

• Expertise in clinical trial documentation

• Understanding of statistical analysis in trials

• Proficiency with document management tools

Drive successful project outcomes through effective writing at Everest Clinical Research.
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