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- Clinical Trial Assistant- CTA-Bulgaria
Clinical Trial Assistant- CTA-Bulgaria
IQVIA Holdings Inc.
Sofia, Bulgaria
Clinical Trial Assistant- Office Based-Bulgaria
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
High School Diploma or equivalent (required)
3 years administrative support experience
Equivalent combination of education, training and experience
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
Written and verbal communication skills including good command of English and Bulgarian language
Effective time management and organizational skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Knowledge of applicable protocol requirements as provided in company training
This position is office-based in Sofia (Bulgaria)
Job posted: 2023-08-08