Local Clinical Trials Assistant, FSP
IQVIA
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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.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
This job is no longer accepting applications
See open jobs at IQVIA.See open jobs similar to "Local Clinical Trials Assistant, FSP" Discover Technata.