Clinical Study Report – Clinical Pharmacology

Barrington James Limited; Remote; GBP 60,000 - 80,000; Part time

Job summary

A leading recruitment agency in the UK is seeking a CSR Writer to assist with Clinical Study Report writing for Phase 1. The ideal candidate will have expertise in report writing, ensuring compliance with regulatory guidelines, and a strong attention to detail. Responsibilities include managing timelines, creating QC reports, and interpreting clinical outputs. If you're a freelancer looking to enter this field, we invite you to apply and discuss further.

Qualifications

• Strong experience in report writing and QC procedures.
• Formal communication skills required.
• Excellent knowledge of formatting in Word.

Responsibilities

• Ensure all deliverables are inspection ready and compliant.
• Maintain planning for writing and QC deliverables.
• Highlight process improvements for collaboration.
• Excel in shell creation and timeline management.
• Create QC reports.
• Interpret clinical and statistical outputs.

Skills

Report writing

Quality Control procedures

Formal communication

Formatting in Word

Tools

Phoenix WinNonlin

Job description

Clinical Study Report (CSR) Writing

We have an amazing client looking for a CSR Writer to support a full Clinical Study Report writing for Phase 1, development and preparation of regulatory Modules (2.7.1/2.7.2). They are looking for strong scientific writing skills, a key attention to detail and inspection‑ready deliverables.

Overview

We have an amazing client looking for a CSR Writer to support a full Clinical Study Report writing for Phase 1, development and preparation of regulatory Modules (2.7.1/2.7.2). They are looking for strong scientific writing skills, a key attention to detail and inspection‑ready deliverables.

Key Responsibilities

• All deliverables are inspection ready and compliant with regulatory guidelines
• Maintain planning for writing and QC deliverables
• Highlight any process improvements to enhance collaboration between CPP and document Service Teams
• Excel in shell creation and timeline management
• Create QC reports
• Interpret clinical and statistical outputs

Skills

• Strong experience in report writing and QC procedures
• Formal communication skills
• Excellent knowledge of formatting on Word

An Ideal Candidate

• Understanding of PK/PD analysis tools
• Working understanding of Phoenix WinNonlin

If you are a contract freelancer in CSR or looking to move into this sector please apply below and I would love to hear from you to discuss the vacancy further.

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