Medical Writer/Senior Medical Writer
4 days left
- Company
- CK Clinical
- Location
- Oxford
- Salary
- £40000 - £45000 per annum
- Posted
- 02 Feb 2021
- Closes
- 04 Mar 2021
- Ref
- 49675
- Contact
- Stephanie Maccioni
- Discipline
- Medical Affairs
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
CK Clinical are recruiting for a Medical Writer/Senior Medical Writer to join a small and highly innovative biotechnology company at their site based in Oxford on a permanent basis.
The Company:
Our client is a highly innovative biotech focused on the development of gene therapies for the treatment of a range of solid tumour cancers administered using their unique proprietary platform.
The Role:
-Writing a range of clinical documents from initiation to completion, producing high quality, clear, accurate and grammatically correct work
-Working closely with the clinical and development teams to discuss, track and propose document updates, and ensure compliance with internal document development SOPs
-Objectively evaluating scientific literature and data to support document development and assisting with literature searches and oncology landscape assessments
-Managing the development and review of documents, and ensuring compliance with timelines and internal and external guidelines/SOPs
-Contributing to and leading (as relevant) document quality control - reviewing data accuracy, formatting and appropriateness of language, and compliance to industry guidelines
Your Background:
-A proven experience working within medical writing
-Life sciences degree and/or relevant academic or industry experience
-Be comfortable assessing trends and patterns in text and statistical data
Apply:
Entitlement to work in the UK is essential. Please quote reference 49675 in all correspondence.
The Company:
Our client is a highly innovative biotech focused on the development of gene therapies for the treatment of a range of solid tumour cancers administered using their unique proprietary platform.
The Role:
-Writing a range of clinical documents from initiation to completion, producing high quality, clear, accurate and grammatically correct work
-Working closely with the clinical and development teams to discuss, track and propose document updates, and ensure compliance with internal document development SOPs
-Objectively evaluating scientific literature and data to support document development and assisting with literature searches and oncology landscape assessments
-Managing the development and review of documents, and ensuring compliance with timelines and internal and external guidelines/SOPs
-Contributing to and leading (as relevant) document quality control - reviewing data accuracy, formatting and appropriateness of language, and compliance to industry guidelines
Your Background:
-A proven experience working within medical writing
-Life sciences degree and/or relevant academic or industry experience
-Be comfortable assessing trends and patterns in text and statistical data
Apply:
Entitlement to work in the UK is essential. Please quote reference 49675 in all correspondence.