Detalhes do emprego
What skills are we lookingfor?Proven experience in medical /medical sciences writing. This should include significantexperience in regulatory medical writing or a mix of experience inregulatory medical writing plus substantial relevant experience ina related role in clinical trials, pharmacovigilance or medicalwriting.Science graduate or equivalentexperience of scientific writing.Goodknowledge of regulatory requirements for clinical trial documentse.g. investigator brochures, clinical study reports and posting ofclinical trial summary results.Excellentproofreading skills and attention todetail.Confident communication skills and ableto foster strong working relationships both internally andexternally.
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