Australia

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)
• 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

Apply here: https://careers.iconplc.com/job/senior-medical-writer-in-uk-reading-jid-35602