Reference Number: JO-2105-468960
Rate: £48,000 – 50,000
Job Type: Permanent
Location: Central London / West End
Regulatory Medical Writer
Location: 100% Home based in UK
Salary: Up to 50,000 per annum + benefits, dependant on experience
CPL Life Sciences are collaborating with a respected scientific regulatory consultancy to hire a junior medical writer to support the preparation of clinical documentation for regulatory submissions. In this role you will work as part of a wider team, responsible for writing assigned clinical documents and supporting client relationships. Other duties will include.
Responsible for writing assigned clinical documents e.g. IBs, CSRs, clinical overviews, module 2 clinical summaries, pediatric plans, orphan designation applications and regulatory briefing documents
Ensuring that all work is complete and of high quality prior to team distribution.
Providing support as appropriate to Business Development/Client Solutions and Medical Writing Services
Reviewing documents drafted from team members to ensure inclusion of all relevant input.
Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent
Must have 3+ years experience in a Medical Writing focused position
Understanding of clinical research, drug development processes and applicable regulatory guidelines
Previously prepared clinical regulatory documentation.
Experienced in managing complex medical writing projects
If you are interested in this role or would like more details please email your CV to Charlie.harris@CPL.com
Remember if this role is not suitable for you please feel free to forward this to anyone you feel would be suitable. If we successfully find a role for your recommendation we will give you 250 in vouchers of your choice.