We are currently working with a successful and well regarded regulatory medical writing consultancy on the recruitment of an experienced medical writer to join their team as the result of company expansion. This company has a background for accommodating home working, so for experienced writers we can offer fully home-based working anywhere within the UK, meaning you can enjoy a healthy work life balance whilst contributing to your overall career progression.
The company in question is a specialist consultancy group working in the areas of regulatory writing and drug safety. Working with prestigious pharma clients, this company has a wealth of experience in their specialist areas and is at the forefront of the prevision of consultancy in these fields. So you can be assured of working with a professional company who can support you in your development.
In this role you will write a range of materials including clinical study reports, CTD modules, IBs, clinical protocols, narratives and PSURs. There will be flexibility on what you get involved in dependant on your specialist areas, so to some extent your work can be tailored to either play to your strengths or to help you gain experience in new areas. You will use your experience to train junior writers, helping with their development within the company.
To be considered for this role it will be necessary to have a strong background in writing clinical study reports, whilst experience in writing clinical summaries and overviews will be an advantage.
For a confidential discussion and to find out more information about this role, or simply to find out more about opportunities available to you within this area, please contact Matthew McGinley from our Medical Communications team on 0207 940 2101 or email@example.com.