Emtex is recruiting a junior medical writer to join its established Regulatory Medical Writing team.
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.Duties and Responsibilities
- In-time generation of clinical documents
- Compilation of clinical documents in accordance with SOPs and GCP
- Gain and maintain knowledge through attendance of workshops and conferences