Sector: Pharmaceutical CRO
Our client is a leading provider of Bioanalytical services to the Pharmaceutical industry.
Due to increased working demand our client is now seeking a Scientific Writer to support with the technical writing for customer project reports.
This role is an out-of-lab position but still requires a good understanding of the pharmaceutical industry along with experience in a regulatory compliant laboratory. You will be expected to utilise this experience to:
- Read and interpret documents, safety rules, SOP’s maintenance instructions and procedure manuals
- Effectively communicate with both laboratory analysts, project managers, study directors and clients
- Able to perform mathematical calculations to present scientific data accurately
- Interpretation and consolidation of technical information
The role would suit an individual with experience working in a Pharmaceutical CRO environment, ideally as a laboratory analyst, who is now looking for an out-of-laboratory position but is still looking to work in close collaboration with research scientists.
Excellent attention to detail, written English and ability to interpret technical scientific information is required.
Good understanding and experience working within to pharmaceutical regulatory compliance – GLP/GCP (FDA, MHRA)
In return, my client offers a permanent position with a competitive annual salary (dependent upon experience) plus competitive benefits package.
For additional information or to submit an application please contact Sam Coxon on 07789 695548 or email your CV and cover letter to firstname.lastname@example.org