Clinsys Clinical Research, Inc.® is a full service contract research organization providing pharmaceutical, biotechnology, and medical device companies with a broad range of clinical research services in support of Phase I - IV drug development. Due to our continued growth we are seeking qualified candidates for the role of Medical Writer in our North Raleigh office. In this role, you will be responsible for combining comprehensive medical knowledge with the ability to compose clear, easily understandable clinical documents. Responsible for the preparation and completion of protocols (including amendments and informed consent forms), clinical study reports, and submission dossiers. The medical writer will observe all regulations concerning medical writing tasks (international, national, sponsor specific or Clinsys specific). The medical writer will communicate with the sponsor and work with clients to ensure that specific requirements with respect to document control and format are met.
Requirements for this position include a Bachelor’s Degree, advanced degree preferred, a minimum of 3-5 years medical writing experience. Experience is a CRO or pharma environment authoring clinical study reports, protocols, investigator brochures, etc. is required.
For immediate confidential consideration, please submit your CV to kthomson@clinsys.com.
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