- To write,
edit and/or manage the production of high quality clinical
documentation for submission to regulatory authorities in support of
marketing applications.
Minimum university life science degree or equivalent Languages: Excellent written and spoken English. Experience/Professional requirement: 1. At least 2 years medicalwriting experience. 2. Good knowledge of statistics and data interpretation and presentation skills. 3. Good knowledge of clinical documentation. 4. Good knowledge of regulatory requirements. 5. Good knowledge of drug development.
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