Clinical Trial Assistant 2

IQVIA; Amsterdam; On-site; EUR 36,000 - 51,000; Full time

Job summary

IQVIA in Amsterdam, Netherlands, is seeking a Clinical Trial Assistant (CTA) to support clinical teams within our global, full-service model. This full-time role involves working closely with CRAs/iCRA and RSU, updating systems, and ensuring documentation meets GCP/ICH standards.

Based in the Netherlands with regular travel to our Breda office (roughly two days per week), you will use MS Word/Excel/PowerPoint and communicate effectively in English and Dutch to keep studies on track and compliant.

Qualifications

• 1 year of CTA experience.
• Fluent written and spoken English and Dutch.
• Strong communication skills.
• Good time management and organizational abilities.
• Able to collaborate with cross-functional teams.

Responsibilities

• Assist CRAs/iCRA and RSU with updating clinical systems tracking site compliance and timelines.
• Assist with preparation, handling, distribution, filing and archiving of clinical documents per SOPs.
• Assist with tracking CRFs, queries and data flow.
• Support distribution of Clinical Trial Supplies and tracking information.
• Serve as central contact for project communications and documentation.

Skills

CTA experience

English and Dutch fluency

Communication

Time management

Organizational skills

Teamwork

Tools

MS Word

MS Excel

MS PowerPoint

Job description

Amsterdam, Netherlands

Full time

R1571201

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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