Similar Jobs
See allSenior Medical Writer
Partner Company
Brazil
Scientific Writing
Regulatory Documentation
Microsoft Office Suite
Principal Medical Writer
Veristat
Global
Medical Writing
Regulatory Affairs
Microsoft Word
Principal Medical Writer
Veristat
US
Medical Writing
Regulatory Documentation
MS Office
Senior/Principal Medical Writer
Jobgether
Europe
Medical Writing
Regulatory Documentation
Project Management
Associate Director, Medical Writing
Acadia Pharmaceuticals
US
Medical Writing
Regulatory Affairs
Clinical Research
Overview:
- Senior medical writing opportunity focused on high-quality scientific publications.
- Produce complex clinical documentation and lead writing strategies.
- Remote role based in Canada, supporting global life sciences.
Responsibilities:
- Lead development of publication deliverables including manuscripts, abstracts, posters.
- Define document strategies and coordinate medical writing activities.
- Mentor writers and contribute to process improvements.
Qualifications:
- At least 6 years of medical/scientific writing experience.
- Strong knowledge of FDA/ICH regulations and AMA style.
- Excellent project coordination and communication skills.
Benefits:
- Fully remote position in Canada.
- Professional development and training opportunities.
- Inclusive, collaborative global environment.
Not disclosed
A global life sciences and healthcare company offering integrated services across the industry. It fosters an inclusive, collaborative culture focused on employee growth, professional development, and delivery of important therapies.