Remote Medical Writer Jobs in Canada

19 Medical Writer jobs in Canada available for remote work from home. Apply for positions such as Medical Writer, Sr Medical Writer, Senior Medical Writer/Principal Medical Writer and more! Discover the best work-from-home or hybrid, full- and part-time jobs.

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Remote Medical Writer Jobs in Canada (19)

Search = Medical Writer Remote in = Canada

Medical Writer

Everest Clinical Research · Full Time · 5 Weeks Ago
Everest Clinical Research
🌎 Canada πŸ’΅ 65000 - 100K per year ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
The Medical Writer is responsible for preparing and quality-checking clinical documents, including protocols, CSRs, and scientific publications. They also handle document e-publishing and may serve as a DMC Administrator to coordinate committee meetings and charters.
ICON plc is hiring for remote Sr Medical Writer

Sr Medical Writer

ICON plc · Full Time · 18 hours ago
ICON plc
🌎 Canada, Germany, United Kingdom, United States ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Senior Medical Writer will lead the development and execution of medical writing strategies for clinical research projects, including the preparation of protocols, CSRs, and regulatory submissions. They will also collaborate with cross-functional teams to interpret clinical data and mentor junior staff to foster a culture of excellence.

Senior Medical Writer/Principal Medical Writer

Precision Medicine Group · Full Time · 4 Days Ago
Precision Medicine Group
🌎 Canada πŸ’΅ $101K - $184K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
Lead the development, writing, and QC review of high-quality clinical study documents including protocols, IBs, and CSRs. Collaborate with sponsors and internal teams to ensure document management complies with regulatory guidelines and company SOPs.

Senior Medical Writer/Principal Medical Writer

Precision for Medicine · Full Time · 4 Days Ago
Precision for Medicine
🌎 Canada πŸ’΅ $101K - $184K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
Lead the development, writing, and QC review of high-quality clinical study documents including protocols, IBs, and CSRs. Collaborate with sponsors and internal teams to ensure document management complies with regulatory guidelines and company SOPs.
Syneos Health is hiring for remote Sr. Medical Writer (Publications)

Sr. Medical Writer (Publications)

Syneos Health · Full Time · 1 Week Ago
Syneos Health
🌎 Canada ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and mentors junior writers to ensure scientific clarity and adherence to regulatory standards.

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Syneos Health is hiring for remote Sr. Medical Writer (Regulatory)

Sr. Medical Writer (Regulatory)

Syneos Health · Full Time · 1 Week Ago
Syneos Health
🌎 Canada, United Kingdom, United States πŸ’΅ $80600 - $175K per year ⭐ 5-10 yrs exp πŸ’Ό Legal Medical Writer
Leads the creation and accurate completion of regulatory medical writing deliverables, including protocols, clinical study reports, and NDA submissions. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and are delivered on time and budget.
Veristat is hiring for remote Principal Medical Writer

Principal Medical Writer

Veristat · Full Time · 1 Week Ago
Veristat
🌎 Canada, France, Germany, Latvia, United Kingdom, United States ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. This involves analyzing and presenting scientific and statistical information according to ICH and company standards.
Veristat is hiring for remote Principal Medical Writer- MedPubs Focus

Principal Medical Writer- MedPubs Focus

Veristat · Full Time · 2 Weeks Ago
Veristat
🌎 Canada, United States πŸ’΅ $132K - $151K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing and presenting scientific information in accordance with industry guidelines and company standards.
Red Nucleus is hiring for remote Senior Medical Writer (Medical Affairs)

Senior Medical Writer (Medical Affairs)

Red Nucleus · Full Time · 3 Weeks Ago
Red Nucleus
🌎 Canada πŸ’΅ 105K - 120K per year ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
The Senior Medical Writer leads the development and scientific accuracy of medical content for pharmaceutical and medical device clients. This includes performing literature research, creating scientific copy, and collaborating with cross-functional teams to ensure regulatory compliance.

Senior Medical Writer

Everest Clinical Research · Full Time · 5 Weeks Ago
Everest Clinical Research
🌎 Canada πŸ’΅ 90000 - 140K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
Author accurate regulatory documents such as CSRs, protocols, and IBs to support clinical trial authorizations and marketing applications. Lead writing projects from initiation to close-out while managing sponsor relationships and performing peer quality reviews.
Veristat is hiring for remote Senior Medical Writer- Clinical Focus

Senior Medical Writer- Clinical Focus

Veristat · Full Time · 5 Weeks Ago
Veristat
🌎 Canada, United States πŸ’΅ $116K - $128K per year ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
Reverba Global is hiring for remote Sr. Medical Writer (CA)

Sr. Medical Writer (CA)

Reverba Global · Full Time · 5 Weeks Ago
Reverba Global
🌎 Canada ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
Develop clear and accurate scientific content across various medical communication deliverables while ensuring strategic alignment and scientific integrity. Lead assigned projects, manage client expectations, and mentor junior medical writers.
Red Nucleus is hiring for remote Medical Writer (Publications)

Medical Writer (Publications)

Red Nucleus · Full Time · 7 Weeks Ago
Red Nucleus
🌎 Canada πŸ’΅ 85901 - 95000 per year ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
The role involves researching, writing, and editing scientific manuscripts, abstracts, posters, and slide presentations for the life sciences industry. The writer will collaborate with the Medical Communications team to deliver high-quality scientific content within designated deadlines.
Trilogy Writing and Consulting is hiring for remote Senior/Principal Medical Writer - Canada

Senior/Principal Medical Writer - Canada

Trilogy Writing and Consulting · Full Time · 8 Weeks Ago
Trilogy Writing and Consulting
🌎 Canada πŸ’΅ 121K - 163K per year ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
Lead the preparation of clinical regulatory documents such as protocols, study reports, and summaries in collaboration with client teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.

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Syneos Health is hiring for remote Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; US/CAN
🌎 Canada, Norway, United Kingdom, United States πŸ’΅ $80600 - $145K per year ⭐ 5-10 yrs exp πŸ’Ό Legal Medical Writer
The role involves leading the clear and accurate completion of medical writing deliverables for studies, managing associated activities, and resolving client comments with minimal supervision. Responsibilities include completing various regulatory documents such as protocols, CSRs, IBs, submissions, and plain language summaries while adhering to regulatory standards and timelines.
Veristat is hiring for remote Principal Medical Writer-nonclinical focus

Principal Medical Writer-nonclinical focus

Veristat · Full Time · 2 Weeks Ago
Veristat
🌎 Canada, United States πŸ’΅ $132K - $151K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They lead project teams, author high-quality submission-level documents, and collaborate with cross-functional teams to ensure regulatory compliance.

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