As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
• Services rendered will adhere to applicable SOPs, WIs, policies, local
regulatory requirements, etc.
• Writes clear and concise clinical submission documents, including clinical study reports,
protocols, clinical overviews, investigator brochures, and summary documents; experience with late
stage health authority responses is a plus.
• Contributes to project plan concerning timelines as well as organization and table layout for a
specific document.
• Ensures that documents meet regulations, and the key messages as defined by the team are clearly
and adequately represented.
• Review and edit documents for consistency, progression, structure, and grammar.
• Review statistical analysis plans and incorporate into clinical study reports or submission
documents, as applicable.
• Drive the document preparation process, manage timelines, receive, and review primary
statistical output, draft, and distribute document for review, compile comments and edits, lead
comment resolution meetings independently.
• Participate in team and client meetings as requested.
You are:
• At least 5 years of pharmaceutical medical writing experience inclusive of clinical study
documents and global clinical regulatory submissions.
• Ability to understand and interpret clinical and scientific data; ability to present results in
an understandable manner to a variety of audiences.
• Knowledge of current requirements and guidelines applicable to submission documents.
• Excellent writing skills.
• Excellent interpersonal and oral communication skills.
• Strong knowledge of MS Word and Outlook, some knowledge of Excel and PowerPoint.
• Project management and organizational skills required including ability to manage timelines and
prioritize multiple projects.
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