Description
JOB ROLE:
The Medical Writer will be working independently, writing the reports of clinical trials and other regulatory documents.
PRINCIPAL RESPONSIBILITIES include:
* Providing additional writing and editing services as required
* Assisting in the production of summaries, pharmacokinetic reports, literature reviews and other documents needed for regulatory submissions
* Assisting in quality control (review) of documents
* Interacting with clients where appropriate
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
* Previous medical writing experience
* Data interpretation skills
PERSONAL SKILLS & ATTRIBUTES:
* Excellent written and oral communication skills
* Strong interpersonal skills
* Good organisational skills
* Computer Literate
* Fluency in English
BENEFITS OF THE ROLE:
This company has an outstanding track record with a style of work that has been rated as the highest in the in the industry. They are committed to providing all the assistance and support you require to enable you to reach your goals. Salaries are competitive and they offer an excellent benefits package including financial and long service awards.
Fforde is acting as a recruitment agency/business.
KEYWORDS:
Medical Writer, Medical Writing, Editor, Editing, Clinical, Clinical Trials, Life Science, Pharmaceutical, CRO, UK