North AmericaFull TimeHealthcare
Remotely
gcpgdprhipaaendnoteama style guideich m11
Job Description
📋 Description
- Lead planning and production of regulatory docs (protocols, ICFs, CSRs)
- Coordinate with authors to translate/write/edit data for publication
- Act as project manager for writing deliverables, track timelines
- Participate in quality control review of others\' documents
- Provide publication support with external executives/designers/editors
- Support study teams with review of training materials when requested
🎯 Requirements
- Undergraduate degree minimum; 3-5 years medical writing exp
- Experience leading development of protocols, ICFs, CSRs
- GCP, GDPR, HIPAA trained
- Advanced EndNote/reference software knowledge
- Familiar with graphical software and figure development
- Adaptable to changing priorities; strong written/oral skills
🎁 Benefits
- Bonus eligible
Back to all jobs
