IQVIA

Scientific Report Writer – Clinical Pharmacology

IQVIA

full-time

Posted on:

Location Type: Office

Location: London • United Kingdom

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Tech Stack

C++

About the role

  • Ensure all deliverables are inspection-ready and compliant with regulatory and internal guidelines
  • Maintain central planning for document writing and QC deliverables
  • Provide recommendations for process improvements to enhance collaboration between CPP and document service teams
  • Drive document shell creation, QC processes, and timeline management
  • Review documents, compile comments, and ensure timely resolution in collaboration with stakeholders
  • Perform QC of reports and manage review cycles
  • Support development of reporting templates, analysis plans, and data transfer plans
  • Draft and review protocols, statistical analysis plans, TLFs/TLF shells, and CSRs
  • Conduct Non-Compartmental Analysis (NCA) using Phoenix WinNonlin 8.3 (preferred but not mandatory)
  • Draft and review programming specifications for studies

Requirements

  • Strong experience in scientific report writing and document QC procedures
  • Proficient in Word templates and document formatting
  • Excellent communication skills (oral and written) in English
  • Familiarity with PK/PD analysis tools and processes, including Phoenix WinNonlin (preferred but not mandatory)
Benefits
  • Competitive salary
  • Flexible working hours
  • Professional development opportunities

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
scientific report writingdocument QC proceduresdocument formattingNon-Compartmental Analysis (NCA)programming specificationsstatistical analysis plansTLFs/TLF shellsdata transfer plans
Soft skills
communication skillscollaborationprocess improvementtimeline management