Lead Medical Writer - ProPharma

Location: Swift Current

Advance your career with Pro Pharma as a Lead Medical Writer based in Canada. This role emphasizes high-quality regulatory documentation and mentoring in a hybrid work environment.

Pro Pharma has been a leader in health and wellness solutions for 25 years, offering a full suite of services to the biotech and pharmaceutical sectors. As a Principal Medical Writer, you'll be pivotal in managing clinical documents and ensuring they meet the highest standards of quality and compliance while collaborating with various functional teams.

Key Responsibilities:

• Create and edit regulatory documents for clinical studies

• Mentor junior writers and oversee their work quality

• Coordinate with subject matter experts for project accuracy

• Manage client communications and project meetings

• Participate in quality control reviews and process improvements

Requirements:

• Bachelor’s degree in a medical or scientific field

• Minimum 7 years of relevant writing experience

• Proficiency in MS Word and regulatory submissions

• Strong attention to detail and project management skills

• Familiar with FDA and ICH regulatory standards

Leverage your expertise in medical writing at Pro Pharma to support transformative healthcare solutions.
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