Scientific Writer – Clinical Pharmacology, Pharmacometrics
IQVIA
full-time
Posted on:
Location Type: Office
Location: Reading • 🇬🇧 United Kingdom
Visit company websiteJob Level
Mid-LevelSenior
Tech Stack
C++
About the role
- Coordinate centralized support for uploading CPP documents into regulatory systems in compliance with global procedures.
- Prepare and review CPP documents for submission, ensuring accuracy, consistency, and inspection readiness.
- Provide scientific writing support for memos, reports, and health authority responses.
- Implement and refine QC processes for CPP documentation, including maintaining QC checklists and tracking comment resolution.
- Collaborate with CPP leaders and cross-functional teams to ensure timely delivery of high-quality documents.
- Support development of templates for CPP reporting, analysis plans, and data transfer plans.
- Maintain central planning and tracking of CPP document deliverables and timelines.
Requirements
- Bachelor’s degree in health sciences, life sciences, or related field.
- Industry experience in scientific writing and document QC.
- Proficiency in Word templates and document formatting.
- Strong organizational and project management skills.
- Excellent written and verbal communication skills in English.
- Familiarity with population PK/PD report writing and review preferred.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
scientific writingdocument QCWord templatesdocument formattingCPP document preparationCPP document reviewQC processesdata transfer plansanalysis planspopulation PK/PD report writing
Soft skills
organizational skillsproject management skillswritten communicationverbal communicationcollaborationattention to detailtimelinessaccuracyconsistencyinspection readiness
Certifications
Bachelor’s degree in health sciencesBachelor’s degree in life sciencesBachelor’s degree in related field