We have a long track record in supporting our customers with dedicated services. Successful candidates will assist in the preparation of a wide range of clinical and regulatory documents, including Investigator Brochures, Clinical Study Reports, Clinical Trial Protocols, Clinical Summaries of Efficacy and Safety and Clinical Overviews. The documents must be of high quality in terms of scientific content, organization, clarity, accuracy, format and consistency, and must adhere to regulatory guidelines and company styles and processes. * Assist more experienced in the preparation of simple documents. * Supported by a Senior or Specialist Medical Writer, write clear, concise, and consistent simple documents compliant with the needs of th
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