Senior Medical Writer

This is an exciting opportunity to join a global Medical writing consultancy that place work life balance and employee wellbeing above all else.

They are hiring for Permanent Medical writers at all levels to join their dynamic global team as they experience a period of rapid growth.

This role will see you become an integral part of your clients clinical development team.

As a Senior Medical writer you will be required to be the lead writer on Clinical and regulatory documents including:  

• Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications.

We are looking to speak to candidates who are keen to progress in their career and develop their skills by working across multiple therapy areas with leading pharmaceutical clients. The ideal candidate will have:

• 3+ Years Regulatory Medical writing experience 
• Experience interacting directly with clients or authors of the documents and coordinating review cycles, meetings, and project timelines.
• Competency in the use of document management systems and associated too.

Founded by Medical Writers they have a strong focus on flexibility and autonomy whilst also offering stability, a constant flow of work in a sometimes-difficult market and a competitive salary package.

If you are looking for your next step as a Medical writer or Senior Medical writer apply today!

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