ICON plc

Senior Medical Writer

ICON plc

full-time

Posted on:

Location Type: Remote

Location: United Kingdom

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Job Level

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