Senior Medical Writer - Regulatory/Clinical - Global CRO - Home based - £negotiable
Senior Medical Writer - Regulatory/Clinical, responsible for researching, creating and editing all documents associated with clinical research.
The Company
My client is a CRO covering multiple therapy areas. Based in the South East, this company have an exciting and broad variety of projects to work on.
- Global, leading CRO
- Home based position
- Great career progression
The Role
The Senior Medical Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research.
- Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc
- Managing multiple projects
- Reviewing all documentation to a high standard
You
To apply for this role as a Senior Medical Writer - Regulatory/Clinical, our client is hoping for someone with the following skills and experience;
- 2 years' experience within a CRO Medical writing position
- Good stakeholder management
- Can work independently
- Degree educated in life sciences
What should you do next?
This Senior Medical Writer - Regulatory/Clinical role is a Regulatory job not to be missed; it encompasses the opportunity to work with new and exciting products within a company who are at the forefront of clinical research. To discuss further, please submit your current CV.
Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.
If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.
