Medical Writer
TLDR
Translate research data into regulatory documents, coordinate authors and specialists, and manage writing deliverables through quality control.
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
Publication Support
Other Writing Support
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
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.
Benefits
Bonus
Remote-Friendly
Fully remote role
Alimentiv delivers specialized clinical research and data services to the healthcare sector, with a strong emphasis on quality assurance and compliance. Our innovative solutions cater to the pharmaceutical and biotechnology industries, accelerating biomarker and drug development through our state-of-the-art lab and clinical imaging software.
- Founded
- Founded 1986
- Employees
- 500+ employees
- Industry
- pharmaceuticals