Description
ICON is seeking a Senior Medical Writer to join their team. The successful candidate will provide scientific and medical/clinical writing support for late-phase projects, servicing an assigned client.
The Senior Medical Writer will work closely with the ICON team and other members of the client account team to ensure the timely delivery of high-quality and scientifically/medically accurate assigned projects.
Responsibilities:
- Write and review study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents, and Study Report
- Develop scientific communication such as abstracts, posters, manuscripts
- Perform quality control for medical writing deliverables
- Interpret statistical results and solicit statistician input for developing study reports, abstracts, manuscripts, and other documents
- Participate in bid-defence presentations representing medical writing activities
Requirements:
- Advanced degree in a scientific discipline, PharmD
- 4+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO, or other healthcare setting
- Proven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry standards
- Outstanding written and verbal interpersonal skills
- Good computer literacy
- Ability to work effectively and cooperatively with cross-functional teams
Rewards & 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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