Senior Medical Writer
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Job Description
Senior Medical Writer creating clinical documents and scientific communications for ICON, a global healthcare intelligence and clinical research organisation. Supporting late-phase projects and client account teams.
Responsibilities:
- Write and review study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report
- Develop scientific communications such as abstracts, posters, and manuscripts
- Perform quality control for medical writing deliverables
- Interpret statistical results and solicit statistician input for study reports, abstracts, manuscripts, and other documents
- Participate in improving the quality assurance system
- Participate in bid-defence presentations representing medical writing activities
- Work closely with the ICON team and client account team to ensure timely delivery of high-quality and scientifically/medically accurate projects
Requirements:
- Advanced degree in a scientific discipline, preferably PhD, PharmD or MD
- 5+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting
- Proven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry standard
- Outstanding written and verbal interpersonal skills
- Good computer literacy
- Ability to work effectively and cooperatively with cross-functional teams
- Legal right to work in the country where the role is based
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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