Clinical Study Report – Clinical Pharmacology
50189
Posted: 13/01/2026
- London , United Kingdom
- Contract
Clinical Study Report (CSR) Writing
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 a strong scientific writing skills, a key attention to detail and inspection ready deliverables.
Key Responsibilities
nhewitt@barringtonjames.com
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 a strong scientific writing skills, a key attention to detail and inspection ready deliverables.
Key Responsibilities
- All deliverables are inspection ready and compliant with regulatory guide lines
- 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 for reports
- interpreting clinical and statistical outputs
- Strong experience in REPORT WRITING and QC procedures
- Formal Communication Skills
- excellent knowledge of formatting on WORD
- an understanding for PK/PD analysis tools
- a working understanding of Phoenix WinNonlin
nhewitt@barringtonjames.com
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