Clinical Trial Assistant - Serbia -one sponsor dedicated
LocationBelgrade, Serbia
Work modehybrid
Typefull-time
EquityIncluded
Company size10,000+ people
First seen1d ago
Last seen1d ago
About the role
Clinical Trial Assistant, Single Sponsor Dedicated
Job Overview:
CTA performs 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. By assisting in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) the Clinical Trial Assistant ensures quality and consistency of study deliverables to time, cost and quality objectives.
Responsibilities
Essential Functions:
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Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems like Trial Master File that track site compliance and performance within project timelines.
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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.
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Assist with periodic review of study files for completeness.
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Assist with contracts preparation and payment handling.
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Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
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Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
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May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
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May take over responsibility for only one administrative segment (for example supplies ), as per project requirements.
Requirements
Qualifications:
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High school or University diploma.
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1+ years of clinical trials administration experience.
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Computer skills including working knowledge of MS Office.
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Written and verbal communication skills including fluency in Serbian and English language.
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Effective time management and organizational skills.
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Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
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The CTA role has a hybrid working mode. Apart from flexibility to work from home, the role may require regular weekly office presence as well.
About the company
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Legal
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.