A staffing agency has an open position for a Telecommuting Senior Medical Writer.Candidates will be responsible for the following: Writing the synopsis and protocol\/CIP of clinical trials\/investigations and\/or of late phase studies\tDeveloping CRF and related documents such as questionnaires and patient diaries\tWriting the integrated Clinical Study ReportMust meet the following requirements for consideration:\tMay be required to travel up to 10%\tBS in a scientific\/technical discipline\tSubstantial experience in pharmaceutical, biological or device development\tProven experience as a Medical Writer and management of regulatory documentation\tExperience with multiple NDA\/IND submissions\tPrevious experience with Medical Devices
Website : http://www.cromsource.com/
Since 1994 CROMSOURCE has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do. At CROMSOURCE we live by our motto – Advise Agree Deliver. This means we leverage our experience and expertise at the early stages of discussions with our clients to freely advise them on the optimal project plan. We then reach agreement with each client on the scope of service, timelines and budget. CROMSOURCE then commit to deliver those services on time and within budget – according to our End-to-End Guarantee. Our commitment to guaranteed delivery is unique in the clinical research environment which is otherwise notable for the routine occurrence of delays and cost overruns. Acting through Pharmaceutical, Medical Device and Staffing Solutions teams, and with a comprehensive portfolio of services, we offer a flexible approach to ensure CROMSOURCE optimally support the unique needs of each client. This could mean providing regulatory consultancy to a small company at the early stages of a medical device development programme, through to provision of full services to a pharmaceutical company performing an international megatrial to support registration of their product. Whatever the size and scope of the project, each receives the same level of attention to detail and commitment to delivery of a high quality service within budget and to timelines agreed.