Broad scientific/ pharmaceutical industry background with 4-6 years of experience in clinical research and/or in pharmaceutical industry. At least 4 years of professional experience as a plain language writer / editor / scientific / regulatory writer within a professional science or health-writing/editing environment, or in journalism and/or in a similar role. Excellent English-language written communication skills. Demonstrated ability to translate complex health information into plain language. Experience writing in plain English and in using heath literacy and numeracy principles. Ability to explain complex material to a non-expert audience. Familiarity with guidance and standards on the design, conduct, and reporting of clinical trials. Ability to work collaboratively in a team environment. Ability to collaborate with writers, technical, and design staff Proven ability to manage workflow involving multiple projects and deadlines Proficiency in Microsoft Office applications and advanced proficiency in Microsoft Word and MS PowerPoint. Minimum Level of Education Required: University Scientific Degree Master or equivalent professional experience
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