Local Clinical Trials Assistant, Fsp
hace 1 mes
**Job Overview**
Support Clinical Research Associates and Regulatory teams in administrative tasks to ensure accurate Trial Master File.
**Key Responsibilities**
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
**Qualifications**
- Bachelors degree in Life Science is good to have
- Upper-intermediate/Advanced level of English
- 3 years of administrative support experience. Prior experience in clinical trials or related is highly valued
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Must be able to visit the sponsor’s offices in Buenos Aires city twice a week.
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