Scientific Writer – Clinical Pharmacology & Pharmacometrics

IQVIA; Badminton; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global healthcare intelligence firm in the UK is seeking a professional to coordinate centralized support for uploading CPP documents into regulatory systems. The role involves preparing and reviewing documents to ensure accuracy, providing scientific writing support, and maintaining quality control processes. Ideal candidates will have a Bachelor’s degree in health sciences or a related field, with industry experience in document QC and scientific writing. Competitive salary and benefits are offered.

Qualifications

• Industry experience in scientific writing and document QC.
• Proficiency in formatting documents using Word templates.
• Familiarity with population PK/PD report writing and review preferred.

Responsibilities

• Coordinate support for uploading CPP documents into regulatory systems.
• Prepare and review CPP documents for submission.
• Provide scientific writing support for memos, reports, and health authority responses.
• Implement and refine QC processes for CPP documentation.
• Collaborate with cross-functional teams to ensure timely delivery.

Skills

Organizational skills

Project management

Scientific writing

Document QC

Verbal communication

Written communication

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