Clinical Trials Professional
Há 5 dias
The Study Coordinator is responsible for providing critical support to clinical trial activities, working closely with Principal Investigators and junior staff.
Key Responsibilities:- Assist Principal Investigators in conducting clinical trials, under the guidance of the Clinical Trials Senior Lead Study Coordinator.
- Compile data, perform routine analyses, and verify accuracy.
- Prepare progress reports and presentations as required by the project.
- Coordinate administrative tasks, including data entry and word processing.
- Resolve data queries and ensure quality control review of source documents.
- Monitor patients throughout the active treatment phase of the study.
- Advanced knowledge of office and administrative practices.
- Proficiency in software applications (MS Word, Excel, PowerPoint, Outlook).
- Expertise in clinical quality improvement principles and methods.
- Excellent written and verbal communication skills.
- Strong organizational and analytical skills.
This position requires a Bachelor's degree in healthcare or a related field and 3+ years of clinical trials experience. A Master's degree is preferred for those with less than 3 years of experience.
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Rio de Janeiro, Rio de Janeiro, Brasil Inside Higher Ed Tempo inteiroOverview The Clinical Trials Co-Director supports the Beacon of Hope clinical trials programs as well as the Personalized Medicine Initiative on a part-time basis. Supervisory Authority None. Nature And Scope Internal contacts may include senior administrators, faculty, students and staff. External contacts may include vendors, consultants and the...
