Principle Medical Writer - Clinical / Regulatory

My client has a position available for a Regulatory/ Clinical Medical Writer to join their team for a 6-month initial contract.
OUTSIDE IR35

Your new role
As the Regulatory/ Clinical Medical Writer, you will provide medical writing services mainly for rare diseases protocols and regulatory submission documents. Similar services may be considered to support the other therapeutic areas as well.

You will work with minimal guidance, taking accountability for delivering regulatory documents, working effectively and closely with key content owners in the relevant functions. Applying project management expertise and contributing to functional excellence through process management.

What you'll need to succeed
In order to apply for the Medical Writer contract, you must possess sufficient experience in clinical and regulatory document writing within the pharmaceutical Industry and be expected to work in autonomy with the project team.

What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK.

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on