Medical Writer
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Job Description
Medical Writer responsible for writing clinical documents like CSRs and protocols at a leading biotechnology company. Collaborating with teams to ensure adherence to standards.
Responsibilities:
- Works with team members and with MW lead oversight to create the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas
- The MW may serve as lead for a compound and is expected to manage and facilitate completion of documents
- Ensures adherence to internal standards and procedures
- Maintains document standardization via model documents/templates and appropriate peer review
- Remains current with writing guidelines and industry standards, participates in educational opportunities, reads professional publications
Requirements:
- Bachelor's degree (advanced degree preferred)
- 1yr of relevant experience
- Awareness of the clinical research process and regulations/guidelines
- Scientific and technical reading, writing, and editing skills
- Organizational, interpersonal and communication skills
- Working knowledge of MS WORD, Adobe Acrobat, PowerPoint, and familiarity with electronic document management systems
Benefits:
- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave)
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