Senior Manager Regulatory Affairs Writing
A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies.
scientific contribution to the development of medical, regulatory and clinical documents to support development programmes. and manage the medical and regulatory writing team along with use of external writing resources when necessary
and develop clinical and medical materials, ensuring that outputs are appropriately referenced and accurate in content and editorial style.
PhD or Masters) preferred.
of writing in the field of Clinical Development within the pharmaceutical industry or contract research organisations
in writing for clinical trials across a range of therapeutic areas and geographies, ideally with immunology/dermatology experience
experience in medical communications, editing and/or publishing would be advantageous
A highly competitive salary, stock options, annual bonus and wider benefits scheme is on offer