Pharmacovigilance Quality Document Reviewer

Your new company My client is a leading biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people''s quality of life, specialising in Oncology, neurology, rare diseases, ophthalmology and immunology.There is an opportunity for a Pharmacovigilance Quality Document Associate to join their Quality Document Review team on an initial 12-month contract.Inside IR35 - PAYE or UmbrellaHybrid - 1-2 days on-site MaidenheadYour new role As a highly motivated individual, your primary focus as a Pharmacovigilance Quality Document Reviewer will be to perform QC (quality review) review to ensure documents authored by the Safety Surveillance and Aggregate Reports (SSA) team or their vendors are of high quality; support process improvement and other SSA functions (e.g., vendor management, SharePoint management).- Source data verification to ensure that all data and methods in all assigned documents agree with source documents, including checking text against database outputs.- Editorial, technical, and scientific reviews for grammatical and stylistic consistency and accuracy- Provide document findings so that appropriate actions can be taken by authors.What you''ll need to succeed - Hold a university degree in a life science or Healthcare- Writing and editing experience, within the pharmaceutical or biotech industry - medical writing, scientific editing and/or publishing.- Familiarity with ..... full job details .....