Senior Regulatory Medical Writer, Leading Consultancy, North West £Negotiable DoE

The Company

This is an exciting time to join an expanding, highly successful consultancy in the leafy suburbs of Greater Manchester. They offer excellent training and development opportunities as well as great career progression opportunities.

• Excellent career progression opportunities

• Great training and development

• Flexible working possible DoE for part of the week (not all)

The Role

As the Senior Regulatory Medical Writer, you will be responsible for;

• Writing and editing regulatory and clinical documents, including protocols, CSRs,

• submission dossiers, PIPs, etc

• Creation of clinical documents in relation to regulatory projects and clinical studies

• Managing and co-ordinating various regulatory writing projects

You

As the Medical Writer (Regulatory), you will have the following experience:

• Previous regulatory / clinical writing experience (min 5 years ideally)

• PhD/MD in medicine, life or health sciences, or pharmacy

• Proven ability to work independently and under pressure, to strict deadlines

What should you do next?

This Senior Regulatory Medical Writer job is a great role and won't be around for long! So don't delay - get in touch today to find out more about either this opportunity of any of our other live jobs within Regulatory Affairs. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.