Scientific Writer: CPP Docs, PK/PD & Regulatory Prep

IQVIA; England; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading global clinical research provider in the United Kingdom is seeking a professional to coordinate the support for uploading CPP documents, prepare and review submissions, and provide scientific writing support. The ideal candidate will have a Bachelor’s degree in health sciences or related fields and experience in scientific writing. Strong organizational skills and proficiency in Word are essential. Join us in improving patient outcomes through innovative treatments.

Qualifications

• 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.

Responsibilities

• Coordinate support for uploading CPP documents into regulatory systems.
• Prepare and review CPP documents for submission.
• Provide scientific writing support for memos and reports.
• Implement and refine QC processes for CPP documentation.
• Collaborate with CPP leaders and cross-functional teams.

Skills

Scientific writing

Document quality control

Project management

Attention to detail

Communication skills (English)

Education

Bachelor’s degree in health sciences or related field

Tools

Microsoft Word

Job description

A leading global clinical research provider in the United Kingdom is seeking a professional to coordinate the support for uploading CPP documents, prepare and review submissions, and provide scientific writing support. The ideal candidate will have a Bachelor’s degree in health sciences or related fields and experience in scientific writing. Strong organizational skills and proficiency in Word are essential. Join us in improving patient outcomes through innovative treatments.