Accenture busca perfiles orientados a SONGndustries will be considered.Thorough knowledge of regulatory requirements including a basic understanding of regulatory requirements in other countries.Thorough understanding of the drug development process.Fluent in local office language and in English, both written and verbal.Fortrea may consider relevant and equivalent experience in lieu of educational requirements.Experience (Minimum Required):Three (3) years of Clinical Monitoring experience.Have a full understanding of Serious Adverse Event (SAE) reporting, process production on reports,



narratives and follow up of SAEs.Advanced site monitoring skills.Advanced study site management skills.Advanced registry administration skills.Ability to work with minimal supervision.Good planning and organization skills.Good computer skills with good working knowledge of a range of computer packages.Advanced verbal and written communication skills.Ability to train and supervise junior staff.Ability to resolve project-related problems and prioritizes workload for self and team.Ability to work within a project team.Works efficiently and effectively in a matrix environment.Valid Driver's License.Preferred Qualifications Include:One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.Local project coordination and/or project management experience.Physical Demands/Work Environment:Travel requirements: *****% overnight.Learn more about our EEO & Accommodations request here .
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📌 Remote Marketing Data Scientist — Ml & Insights (Buenos Aires)
🏢 Fortrea
📍 Buenos Aires