IQVIA
healthcare and biopharma
ClinicalTrialsAssistant1
Neural analysis suggests this role is
optimal for Entry candidates.
“Clinical Trials Assistant 1 at IQVIA. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.. Assisting the clinical team in the preparation, handling, distribution, filing, and archiving of cli”
What You'll Achieve.
improve their probability of success; connecting our scientific, therapeutic and analytics expertise with superior delivery; work on global projects on a variety of therapeutic areas in phases I-III; make an impact in the global research market; working to make a real difference in patient health; accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide
Industry & Context.
must be based in the Netherlands, requirement to commute to a sponsor office in Breda up to 3 times/week
What They're Looking For.
Must Have
At least C1 level of Dutch, At least C1 level of English, High or Secondary School diploma/certificate or country’s educational equivalent (MBO/HBO), approx. 1-3 years administrative support experience within clinical life science, or medical industries
Nice to Have
affinity/experience with finance processes, awareness of applicable clinical research regulatory i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
What You'll Do.
Assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
Assisting the clinical team in the preparation
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.
Supporting CRAs and RSU with preparation
handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
Tracking and management of Case Report Forms (CRFs)
queries and clinical data flow.
Acting as a central contact for the clinical team for designated project communications
correspondence and associated documentation.
Supporting finance processes associated with investigator site payments
How You'll Work.
Team & Collaboration
Working within a smart, dedicated team; collaborative mentoring
Communication Scope
central contact for the clinical team for designated project communications, correspondence and associated documentation
Process & Methodology
project timelines, global projects
Full Job Description
At IQVIA we help healthcare and biopharma companies improve their probability of success. We do this by connecting our scientific, therapeutic and analytics expertise with superior delivery. From advisory through operations, IQVIA and its affiliate companies is the world’s largest provider of product development and integrated healthcare services. **Please note, for this role you must be based in the Netherlands.** Whether you’re beginning or continuing your solid career within administration (finance) or clinical administration, the Clinical Trial Assistant (CTA) is an ideal platform to gain hands-on experience and insight into the world of Clinical Trial Research. Working within a smart, dedicated team, you will thrive under collaborative mentoring and receive structured quarterly reviews on performance, as well as promotion and bonus awards. Award-winning and innovative, we’ll give you access to cutting-edge in-house and mobile technology, allowing you to work on global projects on a variety of therapeutic areas in phases I-III. **WHILE PROJECTS VARY, YOUR TYPICAL RESPONSIBILITIES MIGHT INCLUDE:** \- Assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. \- Assisting 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. \- Supporting CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. \- Tracking and management of Case Report Forms (CRFs), queries and clinical data flow. \- Acting as a central contact for the clinical team for designated project communications, correspondence and associated documentation. \- Supporting finance processes associated wit
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