Clinical Trial Assistant 2

IQVIA Argentina; Amsterdam; On-site; EUR 38,000 - 52,000; Full time

Job summary

IQVIA in the Netherlands is seeking a Clinical Trial Assistant to support CRAs and RSU within our CTAs-driven, full-service model. You will help maintain clinical systems, manage trial documentation, and assist with trial supplies and data flow, while coordinating communications across the clinical team.

The ideal candidate has 1 year CTA experience, fluent English and Dutch, and strong MS Office skills. Regular travel to Breda is required; the role offers professional development and a

Qualifications

• CTA experience (1 year)
• Fluent in English and Dutch
• Knowledge of GCP/ICH guidelines
• Proficient with MS Word, Excel and PowerPoint
• Strong time management and organizational skills
• Ability to build effective working relationships with team members and clients
• Willingness to travel regularly to the Breda office (approx. two days/week)

Responsibilities

• Assist CRAs/iCRA and RSU with updating and maintaining clinical systems to track site compliance and timelines
• Handle clinical documentation and reports according to SOPs; assist with study file reviews
• Assist with Clinical Trial Supplies tracking and documentation
• Manage Case Report Forms, data queries, and data flow
• Serve as central contact for project communications
• Possibly accompany CRAs on site visits for monitoring duties
• Support team with general administrative tasks for trial execution

Skills

CTA experience

English and Dutch fluency

GCP/ICH knowledge

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Time management

Interpersonal skills

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

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.

IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

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.