Scientific Writer – Clinical Pharmacology & Pharmacometrics

IQVIA; Reading; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading global provider of clinical research services is seeking a candidate in Reading to coordinate and support the uploading of CPP documents while ensuring compliance with global procedures. Responsibilities include preparing and reviewing scientific documents, implementing quality control processes, and collaborating with cross-functional teams. A Bachelor’s degree in health sciences or related field is required, alongside industry experience in scientific writing and document quality assurance. The role offers an opportunity to contribute to innovative medical treatments.

Qualifications

• Bachelor's degree in a relevant field is essential.
• Experience in scientific writing and document quality control is required.
• Proficiency in Word templates and formatting is needed.

Responsibilities

• Coordinate support for uploading CPP documents in compliance with procedures.
• Prepare and review CPP documents, ensuring accuracy and consistency.
• Provide scientific writing support for reports and authority responses.
• Implement and refine QC processes for CPP documentation.
• Collaborate with teams to ensure timely delivery of documents.
• Maintain tracking of CPP document deliverables and timelines.

Skills

Scientific writing

Document quality control

Project management

Organizational skills

Communication skills

Education

Bachelor’s degree in health sciences, life sciences, or related field

Tools

Word templates

Job description

Key Responsibilities:

Coordinate centralized support for uploading CPP documents (e.g., population PK/PD data transfer plans, analysis plans, and reports) 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.

Education & Experience 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com