Clinical Trials Assistant 1 - Hybrid

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 with investigator site payments

We look for someone with a strong administrative background and preferrable affinity/experience with finance processes. The ideal candidate has approx. 1-3 years administrative support experience within clinical life science, or medical industries.

WE WILL ALSO BE LOOKING FOR SOMEONE WITH:

a High or Secondary School diploma/certificate or country’s educational equivalent (MBO/HBO)

At least C1 level of

Dutch and English is a must

- This is a hybrid role with a requirement to commute to a sponsor office in Breda up to 3 times/week.

Preferably awareness 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

Are you looking to take the next step and move your career forward with IQVIA? If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.

Connectto great opportunity™

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

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.