Medical Writing jobs in Canada Home Based
- ProductLife GroupRemote
- Fixed term contract
- The Publishing Officer will support regulatory submission publishing activities for global markets as part Publishing project.
- View all ProductLife Group jobs - Remote jobs - Publisher jobs in Remote
- Salary Search: Publishing Officer – VAF salaries in Remote
- ParsonsRemote
- Paid time off
- Vision care
- Dental care
- Life insurance
- Employee assistance program
- RRSP
- Perform other responsibilities associated with this position as may be appropriate such as technical report writing.
- Weekend and evening work will be required.
- Precision Medicine GroupToronto, ON
- $101,800–$152,600 a year
- Paid time off
- Life insurance
- Disability insurance
- BS degree or equivalent in a scientific or medical discipline with relevant writing expertise.
- Contributes to the development and maintenance of medical writing…
- View all Precision Medicine Group jobs - Toronto jobs - Medical Writer jobs in Toronto, ON
- Salary Search: Senior Medical Writer salaries in Toronto, ON
- Precision Medicine GroupToronto, ON
- $101,800–$152,600 a year
- Paid time off
- Life insurance
- Disability insurance
- BS degree or equivalent in a scientific or medical discipline with relevant writing expertise.
- Contributes to the development and maintenance of medical writing…
- View all Precision Medicine Group jobs - Toronto jobs - Medical Writer jobs in Toronto, ON
- Salary Search: Senior Medical Writer salaries in Toronto, ON
- Merit Medical Systems Inc.Remote
- Full-time
- Day shift
- 8+ years of Regulatory Submissions experience in the medical device industry.
- Participates in, supports, and creates Health Canada medical device regulatory…
Clinical Study Builder-Canada
Easily applyInderoRemote- Vision care
- Dental care
- Flexible schedule
- RRSP
- Participates in the definition, writing and updating of Veeva CDMS SOPs.
- The Clinical Study Builder will work closely with data management and statistical staff…
- View all Indero jobs - Remote jobs
- Salary Search: Clinical Study Builder-Canada salaries
- Precision for MedicineToronto, ON
- $92,500–$167,900 a year
- Paid time off
- Life insurance
- Disability insurance
- Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency.
- Dictionary medical coding (MedDRA and WHODrug).
Senior Analyst - Value and Evidence
Easily applyOften replies in 1 dayCostello MedicalVancouver, BC- $90,000–$100,000 a year
- Full-time
- Dental care
- Life insurance
- Designated paid holidays
- Work from home
- Extended health care
- Strong scientific writing skills with the ability to tailor writing style to different audiences.
- At least 2 years’ professional experience in a consulting,…
View similar jobs with this employerAECOMBarrie, ON- $75,000–$105,000 a year
- Full-time
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Experience with proposal writing and/or project management.
- Depending on your employment status, AECOM benefits may include medical, dental, vision, life, AD&D,…
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View similar jobs with this employerOpus RegulatoryRemote- Paid time off
- Vision care
- Dental care
- Life insurance
- Employee assistance program
- Disability insurance
- We offer medical, dental, vision, and prescription drug coverage for employees and their eligible family members.
- IQVIAMississauga, ON
- $97,500–$147,500 a year
- Full-time
- Excellent written and oral communication skills including grammatical/technical writing skills.
- Cronos est la branche mondiale d’IQVIA spécialisée dans…
- IQVIAMississauga, ON
- $103,000–$153,000 a year
- Full-time
- Good regulatory and/or technical writing skills.
- Mississauga, Canada | Full time | Home-based | R1545093.
- Superviser l’exécution de l’activation des centres (y…
- InderoRemote
- Permanent
- Vision care
- Dental care
- Company pension
- Flexible schedule
- Excellent understanding of all services offered by a CRO in a clinical project (medical and scientific writing, clinical trial management, clinical monitoring,…
Medical Monitor (Canada Board-Certified Gastroenterologist)
Easily applyOften replies in 1 dayPSI CRORemote- $170,000–$185,000 a year
- Full-time
- Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable.
- Proficiency with MS Office applications.
- FortreaToronto, ON
- $140,000–$180,000 a year
- Full-time
- Liaise with medical, clinical, data management, regulatory and QA personnel regarding safety issues, as appropriate.
- RN + 10 yrs. relevant experience.
- Nucs AIToronto, ON
- Flexible schedule
- Active, unrestricted medical license in the US.
- We collaborate with leading medical institutions and pharmaceutical companies globally to achieve groundbreaking…
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Job Post Details
Publishing Officer – VAF - job post
Job details
Job type
- Fixed term contract
Full job description
The Publishing Officer will support regulatory submission publishing activities for global markets as part Publishing project. The role focuses on the preparation, compilation, and publishing of regulatory submissions in multiple electronic formats, ensuring compliance with regional regulatory authority requirements and internal quality standards.
This position is a replacement role with long-term project visibility (3+ years) and offers the opportunity to work in a global regulatory environment
Key Responsibilities
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Perform regulatory publishing activities in eCTD, NeeS, ePaper, and ACTD formats.
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Support submissions across EU, US, Canada, Australia, GCC, ASEAN, and other global regions.
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Compile, publish, and validate regulatory submissions in line with health authority requirements.
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Ensure accuracy, consistency, and technical compliance of published submissions.
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Coordinate and plan assigned publishing projects in collaboration with internal stakeholders.
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Perform quality checks and address validation findings prior to submission.
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Maintain submission documentation and ensure proper version control.
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Work effectively within defined timelines while managing multiple submissions.
Required Qualifications
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Bachelor’s degree in Life Sciences or a related discipline.
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3+ years of experience in Regulatory Affairs / Regulatory Operations with hands-on eCTD publishing exposure.
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Experience working on international, EU, and RoW submissions.
Technical Skills
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Experience with eCTD and NeeS publishing.
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Strong knowledge of electronic document management systems (eDMS).
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PDF preparation and editing using Adobe Acrobat Pro.
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Hands-on experience with DocuBridge (Preferred
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Familiarity with ISI Toolbox / Evermap (bookmarks, hyperlinks, TOC creation).
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Basic understanding of Regulatory Affairs processes and submission lifecycle.
Soft Skills & Competencies
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Highly organized and methodical approach to work.
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Strong attention to detail and quality mindset.
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Ability to manage priorities and work under tight timelines.
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Adaptable and comfortable working in a global, remote environment.
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Clear communication and collaboration skills.