Senior Medical Writer
ICON plc
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
Visit company websiteExplore more
Job Level
Tech Stack
About the role
- Provide scientific and medical/clinical writing support for late-phase projects
- Write and review study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report
- Develop scientific communication materials such as abstract, poster, manuscript
- Perform quality control for medical writing deliverables
- Interpret statistical results and collaborate with statisticians
- Improve the quality assurance system
- Participate in bid-defence presentations for medical writing activities
Requirements
- Advanced degree in a scientific discipline, preferably PhD, PharmD, or MD
- 5+ years of professional experience in Medical Writing
- Proven knowledge of ICH/GCP and GPP guidelines
- Outstanding written and verbal interpersonal skills
- Good computer literacy
- Ability to work effectively and cooperatively with cross-functional teams
Benefits
- Competitive salary packages
- Annual bonuses reflecting performance goals
- Range of health-related benefits
- Competitive retirement plans
- Life assurance
- Various annual leave entitlements
- Health insurance offerings
- Global Employee Assistance Programme
- Flexible country-specific optional benefits
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical writingscientific writingquality controlstatistical interpretationscientific communicationprotocol writingdata collection document writingstudy report writingabstract writingmanuscript writing
Soft Skills
interpersonal skillswritten communicationverbal communicationcollaborationteamworkquality assurancepresentation skills
Certifications
PhDPharmDMD