Clinical study report writing and quality control define this Medical Writer role at Everest, based in Toronto/Markham or remotely anywhere in Canada.
As a Medical Writer, you will prepare clinical documents and scientific publications for pharmaceutical clinical trials. The work requires medical writing, clinical trial understanding, statistical interpretation, and detailed document quality control. You will support project teams and client deliverables across assigned timelines.
Key Responsibilities:
- Lead preparation of clinical documents and scientific publications
- Interpret study results using protocols and statistical outputs
- Perform quality control on clinical reports and references
- Finalize documents for Sponsor delivery within timelines
- Perform literature searches supporting senior medical writers
Requirements:
- Advanced degree in clinical, medical, or life sciences
- At least two years of medical writing experience
- Pharmaceutical clinical trial environment experience
- Understanding of GCP/ICH guidelines, including E3 requirements
- Comprehensive Microsoft Office and Adobe Acrobat skills
Apply medical writing, clinical trial knowledge, statistical interpretation, and quality control expertise to Everest deliverables across Canada.
Clinical Study Report Medical Writer in Toronto employer: Everest Clinical Research Corporation
Everest Clinical Research is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the clinical trials sector. With opportunities for mentorship and professional growth, employees are empowered to lead impactful projects while enjoying the flexibility of remote work or the vibrant atmosphere of our Toronto/Markham offices. Our commitment to regulatory excellence and proactive client engagement ensures that every team member contributes to meaningful advancements in healthcare.
Contact Details:
Everest Clinical Research Corporation Recruitment Team
