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.
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
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 skillset
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)