Senior Medical Writer — Regulatory Lead & Mentor

MMS Holdings Inc; Calgary; Remote; CAD 80,000 - 120,000; Full time

Job summary

MMS Holdings Inc. in Calgary, Canada is seeking an experienced Medical Writer to evaluate literature, design studies, and prepare regulatory documents such as protocols, investigator's brochures, and study reports.

You will manage writing tasks, meet timelines, mentor junior writers, and liaise with clients to coordinate projects, ensuring scientific rigor and consistent styles per templates and guidelines.

Qualifications

• At least 3 years of pharmaceutical industry experience in regulatory writing.
• Ability to author clinical study reports and regulatory documents with high quality.
• Experience leading writing teams and coordinating with clients.

Responsibilities

• Critically evaluate literature to select material for study design and regulatory use.
• Write and edit clinical development documents (protocols, brochures, study reports, consent forms).
• Maintain timelines and project workflows; mentor other writers.
• Communicate effectively with clients and internal teams on project needs.
• Ensure writing aligns with client templates and regulatory guidelines.

Skills

Regulatory writing

Medical writing

Project leadership

Communication

Organizational skills

Education

Bachelor's, Master's or PhD in scientific/medical field

Tools

MS Word

Excel

PowerPoint

Job description

MMS Holdings Inc. in Calgary, Canada is seeking an experienced Medical Writer to evaluate literature, design studies, and prepare regulatory documents such as protocols, investigator's brochures, and study reports.

You will manage writing tasks, meet timelines, mentor junior writers, and liaise with clients to coordinate projects, ensuring scientific rigor and consistent styles per templates and guidelines.