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
Qualifications
5+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting
PhD (Medical field or biology preferred)
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
