ICON Hiring Senior Medical Writer
The Role
- Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.
- Responsible for developing scientific communication such as abstract, poster, manuscript, etc.
- Responsible for performing quality control for medical writing deliverables
- Responsible for interpreting statistical results and for soliciting statistician input for developing study reports, abstracts, manuscripts, and other documents as required
- Participating in the improvement of the quality assurance system
- Responsible for participating in bid defense presentations representing medical writing activities
To Perform This Job Successfully, You Will Need
- 5+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting
- Masters’ degree or higher degree in a scientific discipline (medical field or biology)
- Bilingual – Korean and English
- Proven knowledge of ICH/GCP guidelines or other meaningful guidelines or industry standard
- Outstanding written and verbal interpersonal skills
- Good computer literacy
- Ability to work effectively and cooperatively with other team members