Clinical Trial Assistant 2

IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.

Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.

Please note, for this role you must be based in the Netherlands.

As a Clinical Trial Assistant within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CTAs.

With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

Essential Functions of a Clinical Trial Assistant (CTA)

• Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. 
• Assist the clinical team in 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/iCRAs 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 and with required approval.
• May perform assigned administrative tasks to support team members with clinical trial execution.

Required Knowledge and Skills

• Regular travel to the Breda office is required, typically two days per week
• At least 1 year of CTA experience
• Good written and verbal communication skills including fluent command of English and Dutch language
• Strong understanding of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of applicable protocol requirements as provided in company training
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
• Effective time management and organizational skills
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.