Senior Regulatory Writer

☞ RemoteWorker UK

View: 101

Update day: 18-05-2024

Location: Newcastle-under-Lyme West Midlands

Category: Marketing / PR Printing / Publishing

Industry: Staffing Recruiting

Position: Mid-Senior level

Job type: Full-time

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Job content

Job Summary We are an oncology focussed pharmaceutical company looking for a Senior Medical Writer to join our small close-knit team and work closely with clinical and regulatory teams. The ideal candidate would have worked with a broad range of clinical documents. This role can be home based anywhere - remote. Job Overview Who are we: We are an oncology focussed pharmaceutical company with one product on the market and a number of studies going through phase I, II & III. Our writing team is currently 6 people who work in a supporting and collaborative environment and we are looking for someone who is looking to be an integral part of this team. Key Responsibilities Author of clinical and non-clinical documentation: CSR, protocol, IBs, CTD Modules 2.5 & 2.7 and briefing books Work closely with regulatory, clinical and biometrics teams to ensure effective collaboration and data sharing Lead the development and roll-out of project timelines Liaise with external vendors where appropriate Skills Required Key Skills: Must have at least 3 years of industry regulatory writing and clinical medical writing experience The ideal candidate would hold a Bachelors, Masters, or PhD. in scientific, medical, clinical discipline Understanding of clinical data Exceptional writing skills are a must Good spoken and written English Commutable locations: Home based anywhere in Europe or South Africa - remote This role is suitable for: Medical Writers and Senior Medical Writers
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Deadline: 02-07-2024

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