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The Scientific Writer is the medical writing expert responsible for the research, writing and editing of regulatory documents. The incumbent will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Responsibilities will include assuring quality and timely preparation of clinical documents across all therapeutic areas, including clinical study reports, clinical study protocols, investigator's brochures, and clinical summaries and overviews.
Qualifications:
Requirements: Bachelor's degree or equivalent, with at least six years experience in scientific discipline and a minimum of four years in Medical Writing. Master's degree, PhD, or equivalent with a minimum of two years previous industry experience. Demonstrated working knowledge of scientific principles. Excellent written and oral communication skills in English. Familiarity with all phases of medical research and ability to learn new medical concepts quickly. Familiarity with statistics and experimental design. Ability to summarize complex data and identify relationships.
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