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Medical Writer I

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About the role

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MEDICAL WRITER
 
As a core member of the Medical Writing and Publishing team you will be writing the reports of clinical trials and other regulatory documents (including patient narratives for serious adverse events and drop-outs due to non‑serious adverse events) according to ICON- or client-specified formats
 
RESPONSIBILITIES:
  • Assist in the production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews, and other documents needed for regulatory submissions
  • Interpret and summarise data from bio statistical summary tables and listings accurately, precisely, and concisely into narrative text
  • Liaise with internal groups, i.e. Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical, and Quality Assurance to obtain the necessary information and to ensure the timely implementation of activities related to the production of reports
  • Interact with clients with support from the Senior Medical Writer
 
 REQUIRMENTS:
  • Life science or writing qualification (preferably at post-graduate level)
  • Knowledge of clinical trial processes
  • Excellent writing and oral communication skills, problem-solving ability, data‑interpretation skills, strong interpersonal skills, ability to plan and organise
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