Clinical CPP Writer - Pharmacometrics & Regulatory Docs

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

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.