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Senior Manager, Medical Writing
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Consultant in Histopathology
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Consultant in Renal Medicine
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Machine Operator
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Consultant in Histopathology
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Senior Manager, Medical Writing - Cambridge, Cambridgeshire, United Kingdom - Pharma Partners Recruitment Ltd
Description
Senior Manager Regulatory Affairs WritingA 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.Responsibilities:
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 necessaryand coordinate the development of cross-functional documents to ensure completion to develop clinical and medical materials, ensuring that outputs are appropriately referenced and accurate in content and editorial style.
PhD or Masters) writing in the field of Clinical Development within the pharmaceutical industry or contract research organisationsin writing for clinical trials across a range of therapeutic areas and geographies, ideally with immunology/dermatology experienceexperience in medical communications, editing and/or publishing would be advantageous Salary and benefits:A highly competitive salary, stock options, annual bonus and wider benefits scheme is on offerTo apply for this position or hear further details then please contact Matt Thomas via matt.