Medical Writer

Job not on LinkedIn

🔥 0 minutes ago

🇨🇦 Canada – Remote

💵 $69k - $115.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

👻 Ghost score 2%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Alimentiv

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.

📋 Description

• Provide medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation • Research, write, review, and edit scientific information • Coordinate document reviews with authors • Conduct reference searches and verify citations • Translate research data and findings into regulatory documents and presentations, including protocols, investigator brochures, clinical study reports, and informed consent forms • Track progress and timelines for assigned writing projects • Perform document quality control reviews when requested • Lead content planning and production of regulatory documents • Coordinate specialized content with authors and technical specialists • Translate, write, edit, and proof data and content for finished documents • Act as project manager for writing deliverables, track timelines, and provide progress reports • Participate in quality control review of documents written by other authors • Liaise with external publication executives, illustrators, designers, and editors • Support study teams with review, editing, or proofreading of study documents and templates • Assist with writing or reviewing training materials and work instructions

🎯 Requirements

• Minimum of an undergraduate degree (advanced degrees preferred) • 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

🏖️ Benefits

• Bonus • Full-time, permanent employment