Lead Medical Writer, Clinical Trials & Publications

Everest Clinical Research Corporation; Toronto; Hybrid; CAD 65,000 - 100,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life & AD&D insurance

Short- and long-term disability

Tuition reimbursement

Fitness reimbursement

Employee assistance program (EAP)

Pension plan

Paid time off

Job summary

Everest Clinical Research Corporation seeks a Medical Writer for its Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada per our Work from Home policy.

The role involves leading medical writing deliverables, performing QC on study documents, and supporting regulatory submissions across multiple therapeutic areas. Strong writing, editing, and project coordination skills are essential.

Qualifications

• Advanced degree in Clinical/Medical/Life Sciences or equivalent.
• 2+ years of medical writing experience in pharma/clinical trials.
• Experience with medical writing for regulatory submissions is preferred.

Responsibilities

• Lead medical writing deliverables and ensure adherence to Everest or Sponsor writing styles.
• Perform QC on clinical documents (protocols, CSRs, PK, reports, manuscripts) for accuracy and consistency.
• Conduct literature searches to support medical writing.
• Publish documents to Word/PDF, create hyperlinks/bookmarks, update TOCs and pagination.
• Coordinate TCL/DTM packaging for other teams; assist DMC with governance tasks as needed.
• Plan and manage deliverables and timelines per project requirements.

Skills

Interpersonal skills

Communication skills

Detail-oriented

Multitask/document management

Education

Ph.D. preferred in clinical/medical/life sciences

Master's degree with substantial experience

Tools

Microsoft Office

Adobe Acrobat

TRS Toolbox pharma edition

Job description

Everest Clinical Research Corporation seeks a Medical Writer for its Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada per our Work from Home policy.

The role involves leading medical writing deliverables, performing QC on study documents, and supporting regulatory submissions across multiple therapeutic areas. Strong writing, editing, and project coordination skills are essential.