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Scientific Editor Jobs in Quebec (NOW HIRING)

... editing scientific information, coordinating document reviews with authors, conducting reference searches and verifying citations, translating research data and findings into regulatory documents ...

Technical Writer

Montreal, QC · On-site

CA$500/day

Act as an editor to ensure consistency in training documentation across the IPMS product; * Translations to French of technical documents Qualifications: * Bachelor or Bachelor of Science in ...

Our technology empowers scientists to generate precisely modified primary and immortalized cell ... editing. What You'll Do * Build, test, and troubleshoot microfluidic devices * Assist in the ...

Technical Writer

Montreal, QC · Hybrid

CA$500/day

Act as an editor to ensure consistency in training documentation across the IPMS product; * Translations to French of technical documents Qualifications: * Bachelor or Bachelor of Science in ...

Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans ... Concevoir, rédiger, réviser et éditer des plans d'étude, des amendements et des calendriers ...

... editing, and reviewing documentation and training materials, in accordance with Acumatica's AI ... A degree in English, technical writing, communications, or computer science or alternative ...

Grace a une expertise inegalee en ingenierie, en services-conseils et en sciences, nos esprits ... Corriger et editer les rapports pour garantir l'exactitude, la clarte et la qualite. Gerer les ...

When you join us, you'll be part of a global team harnessing the power of scientific testing and ... Superior computer skills in Microsoft Office Suite and photo editing software; * Exceptional ...

Grace a une expertise inegalee en ingenierie, en services-conseils et en sciences, nos esprits ... Corriger et editer les rapports pour garantir l'exactitude, la clarte et la qualite. Gerer les ...

Bachelor's degree in Computer Science, Engineering, or equivalent experience. * Expert-level ... Editor's Choice and Google Play's Best Game of the Year. Founded in 2006, Kabam has studios and ...

Scientific Editor information

What does a scientific editor do?

A Scientific Editor reviews, edits, and formats scientific manuscripts to ensure clarity, accuracy, and adherence to publication standards. They work with researchers and authors to refine content, improve readability, and verify data or references. Scientific Editors may also manage peer review, provide feedback, and ensure the manuscript meets journal or publisher guidelines. Their role helps enhance the quality and impact of scientific publications.

What are the key skills and qualifications needed to thrive as a scientific editor?

To thrive as a Scientific Editor, you need a strong background in scientific research, advanced written communication skills, and typically an advanced degree (such as a Ph.D. or MSc) in a relevant field. Familiarity with manuscript submission platforms, reference management tools, and editorial standards like AMA or APA style is important. Strong attention to detail, the ability to provide constructive feedback, and effective time management are valuable soft skills in this role. These qualities ensure accuracy, clarity, and efficiency in the publication process, ultimately upholding the integrity of scientific communication.

What are popular job titles related to Scientific Editor jobs in Quebec?

For Scientific Editor jobs in Quebec, the most frequently searched job titles are:

Infographic showing various Scientific Editor job openings in Quebec as of August 2026, with employment types broken down into 85% Full Time, and 15% Part Time. Highlights an 92% In-person, and 8% Hybrid job distribution.

Medical Writer

Alimentiv

Montreal, QC • On-site

Full-time

Posted 6 days ago


Job description

In this role you will be providing medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation, which may include researching, writing, reviewing and editing scientific information, coordinating document reviews with authors, conducting reference searches and verifying citations, translating research data and findings into  regulatory documents (protocols, investigator brochures, clinical study reports, informed consent forms, etc.) and presentations on a timely basis and in alignment with industry, regulatory and academic style and content guidelines and standards. Track progress and timelines for assigned writing projects. Perform document quality control review when requested. Assist with writing or review of relevant training materials or work instructions as needed.

Clinical Research/Academic Writing Support
  • Lead the content planning and production of regulatory documents (protocols, investigator brochures, clinical study reports, informed consent forms, etc.) in alignment with established standards and guidelines
  • Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience.
  • Act as the project manager for writing deliverables and regularly track timelines and provide progress reports to stakeholder(s).
  • Participate in quality control review for documents written by other authors when requested.
Publication Support
  • Act as primary contact and liaison with external publication executives, illustrators, designers, and editors, representing the Scientists/Investigators, Sponsors and/or the corporation with external specialists to select publication content, address content change requests, complete written revisions and/or resolve competing content requirements.
Other Writing Support
  • Upon request, support study teams with review, editing or proof-reading of study documents or templates, such as charters, informed consent forms, or study plans (safety, statistical analysis, etc.).
  • Assist with writing or reviewing relevant training materials or work instructions when requested.
Qualifications
  • Minimum of an undergraduate degree (advanced degrees preferred) and 3-5 years of relevant experience in medical writing.
  • Previous experience leading the development of protocols, ICFs, and CSRs
  • Trained in GCP, GDPR, and HIPAA
  • Advanced knowledge of EndNote/reference software
  • Familiarity with graphical software and figure development is an asset.
  • Ability to adapt to shifting priorities and assignments.
  • Highly refined written and oral communication skills.
  • Demonstrated ability to work with diplomacy and tact.
  • Previous experience/knowledge of Gastroenterology is an asset.
  • Familiarity with ICH M11 and the AMA Style Guide is an asset.
  • Continuous improvement mindset and willingness to embrace new technologies where appropriate
$69,000 - $115,500 a year
+ bonus
Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn't feel right, we encourage you to verify before responding.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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