Regulatory Medical Writer – Home Based
Our Client is a specialist CRO based in Sussex and they are looking for a Regulatory Medical Writer to join their Oncology team on a permanent. In this position you will primarily focused on writing Clinical trial Applications and amendments & Investigational Medicinal Products Dossier for Oncology projects.
- Clinical study protocols and protocol amendments
- Interim and final reports for clinical studies
- Annual study reports
- Investigator brochures
- Patient Informed Consent forms
Some familiarity with industry principles of drug safety, US and international regulatory guidelines, drug development, biostatistics, pharmacology, clinical trial methodology, and oncology would be advantageous although not mandatory. The position requires proven ability to meet deadlines and be results-oriented. Ability to manage critical issues on multiple projects simultaneously is key. The person in this capacity will be a team-player, highly organized, self-motivated, and extremely detail-oriented. He / she will have strong oral and written communication skills, excellent interpersonal skills, and advanced computer literacy (MS Word is required).
Contact: Elliot Brackpool
Keywords: Contract, Regulatory, oncology, pharmaceutical, Regulatory Affairs, Medical Writer, London, EU, London, Home based
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