Clinical CPP Writer - Pharmacometrics & Regulatory Docs

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

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.