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Precision Medicine Group

Senior Medical Writer/Principal Medical Writer

RemoteUnited Kingdom only
Published
Role
Content
Experience
Senior
Salary not disclosed
Check eligibility

Open to GB only. Set where you work from to check your eligibility.

No BS summary

Senior/Principal medical writer for clinical study documents in a sponsor or CRO setting. Requires 5+ years as a Senior Medical Writer or 7+ years as a Principal Medical Writer, scientific/medical degree, regulatory knowledge, and UK remote eligibility.

Core skills

Medical WritingClinical Study Documents

Required skills

Microsoft WindowsMicrosoft TeamsMicrosoft WordMicrosoft ExcelAdobe AcrobatMicrosoft PowerPointICHFDAGCPEudraCTCT.goveCTD

What you'll do

  • Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidance's
  • Ensures smooth and effective document management from start to finish (ie, from template to final, approved version) in collaboration with Sponsor, external vendors, and/or internal Precision project teams/departments
  • Ability to independently formulate key messages from clinical study data
  • Ability to author complex content using knowledge/skills and understanding of processes
  • Ability to communicate clearly and concisely both in writing and verbally with internal and client teams
  • Contributes to the development and maintenance of medical writing processes, SOPs, templates, and work instructions for key documents
  • Performing literature-based research to support writing activities
  • Other duties as assigned

What they require

  • BS degree or equivalent in a scientific or medical discipline with relevant writing expertise
  • 5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer.
  • Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of development
  • Impeccable attention to detail and ability to complete writing assignments in a timely manner
  • Ability to work effectively in a fast-paced environment with multiple high-priority projects with no instruction on routine work and minimal instruction on new assignments
  • Excellent problem-solving skills
  • Preferred: Advanced degree (MS/PhD)
  • Preferred: Oncology and/or rare disease experience (especially protocol and CSR development)
HealthcareEnterprise

What people say about this company

3.3/ 5

Details

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Salary not disclosed