Senior Regulatory Writer

3 weeks ago


United Kingdom Meet Full time

Senior Med/Reg Writer - Clinical Trial Documentation/Submissions - Global Med Comms/Regulatory Agency - Remote - UK
Thrilled to be partnering our client, a Global Medical Communications agency, to support them in their search for a Senior Regulatory Writer, to join their growing team in the UK.

We are looking for an experienced Reg Writer with strong background with the preparation of Clinical Regulatory Documents such as CSR's, PSUR's and CTD's - you will also be responsible for client services, working closely with them and contributing to the strategic planning of Regulatory Submissions.

Our client is a full service, global healthcare communications agency who deliver a vast range of communication planning, publications, medical meetings, digital programmes, health economic and regulatory services to pharmaceutical companies.

They are an organisation which has grown solidly since their inception nearly 20 years ago and are proud to still be working with a number of clients joined with them from the beginning - this further demonstrating the quality of the work and relationships they hold in high regard.

As an organisation with a significant remote workforce, they invest time and money into creating an environment in which you feel engaged and part of the team, as well as challenged and rewarded to grow and develop.

If you're in a role where you feel you are overworked or underappreciated or both and looking for a people centric organisation to kick start your career, let's talk



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