Medical Writer

Regulatory Professionals
North East England
On Application
27 Sep 2017
03 Nov 2017
Contract Type
Full Time
Medical Writer Freelance Part Time - 2 days per week 12 Month Contract East Yorkshire or Homebased Regulatory Professionals are recruiting on behalf of a leading global pharmaceutical company The firm have operations in over 60 countries, with headquarters in the UK, Singapore, Dubai and Amsterdam and sales covering every continent in almost 200 countries and are looking for a Medical Writer to join the team on a contract basis. Responsibilities * Support the writing, editing and reviewing of diverse Regulatory and Clinical Documents required for global product development and registration activities. These include but are not limited to: briefing documents, common technical document (CTD) clinical overviews and summaries, switch applications, integrated summaries of safety and efficacy, clinical evaluation reports and other Regulatory documents. * Provide input and edit/review Clinical documents such as Study Protocols, Investigator's Brochures and Informed Consent Forms * Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation * Review, improve and maintain existing documentation; prepare where appropriate * Systematic literature searches/reviews as necessary * Understand clinical, regulatory and medical data for the product and competitors, provide the team with innovative stimulus about the product portfolio Experience * Bachelor's Degree associated to healthcare or the life sciences * Excellent written/oral communication skills. Ability to adapt style and content for different target audiences. Experience in preparing medical or scientific documents (medical writing) to a high standard is essential and experience of working in or for the Healthcare OTC industry is highly desirable. * Ability to develop appropriate research strategy and conduct a systematic review of available published data including retrieval, critical appraisal and appropriate citing of literature * An understanding of healthcare compliance and guidelines is desirable * Knowledge of consumer healthcare is a distinct advantage. Good understanding of the commercial drivers of the business * Experience of researching and scanning various internal and external databases * Skilled with MS Word and competent in MS Excel and the use of bibliography databases. Experience with Document Management systems If you are looking for you next contract positions and available for a 12 month contract then please get in touch ASAP, this is a great opportunity to work for a global pharmaceutical company Opportunities to work for this business on a contract basis do not come about very often and therefore if you are interested please send your CV urgently to regulatory professionals or call to have a confidential chat about your search : Medical Writer, Regulatory, Clinical Documents, Regulatory Documents, Contract, Part time, OTC