Clinical Trial Assistant 1 Exclusive for People With Disabilities

This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply you can apply for other vacancies within IQVIA jobs.

Job Overview
Perform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.

Essential Functions
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
Bachelor Degree in Life Science or Health Care.
Ideally 1 years experience in a healthcare environment or equivalent combination of education training and experience. Administrative Support experience is highly valuated.

Upper Intermediate - Advanced level of English.

Hybrid Role: Offices are in Bogota Colombia.
Computer skills including working knowledge of Microsoft Word Excel and PowerPoint.

Please submit your updated CV and Medical Inform when applying.

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