Senior Medical Writing Associate

Job Details

Company

A top global pharmaceutical company is seeking a new Senior Medical Writer for its Buckinghamshire site.


Role

- Compiles, assembly and quality control review of clinical documents and performing other medical writing tasks as needed.
- Adhere to all relevant regulations including ICH, PhRMA and CFR guidelines, SOPs, etc.
- Prepares clinical study reports for phase I-III clinical studies in support of regulatory submission of drugs and biologics worldwide.
- Serves as lead writer on regulatory filings and other medical writing projects.
- Works with various departments to ensure that all necessary information is provided, organized and summarized efficiently.
- Ensures that clinical study reports accurately reflect study results and coincide regulatory requirements.


Qualifications

- Degree or higher in a science or health-related discipline.
- Prior experience of working as a medical writer.
- Experience of clinical regulatory writing.
- Ability to travel <10% of the time.


How to Apply

To apply, please click on the Apply button. Ideally, please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call me (Kevin Hansberry) on +44 (0) 207 440 0636 or upload your CV on our website. Full description available on request.

Please note that not all of our vacancies are advertised. To register as a priority candidate, please upload your CV on our website with a short description of what you are looking for or call 0800 988 4437. We will then contact you with relevant roles: www.proclinical.co.uk. We regard all correspondence as confidential.

Proclinical is a specialist Employment Agency and Recruitment Business, providing employment opportunities within major companies in the Pharmaceutical and Biopharmaceutical industries across Europe.