Senior Clinical Trial Assistant - Sponsor dedicated - Netherlands- Hybrid (m/w/d) at IQVIA, Amsterdam, NY
Senior Clinical Trial Assistant - Sponsor dedicated - Netherlands- Hybrid (m/w/d) at IQVIA in Amsterdam, NY. Full-time. Apply with swipeandhired.
Why Join Clinical Functional Service Partnerships (CFSP)?
At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. You'll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve.
Through our long-standing partnerships with the world's leading pharmaceutical and biotechnology companies, you'll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing.
Build Your Future with IQVIA
If you're looking to build a career in clinical research, this is where it starts. As a Senior Clinical Trial Assistant within Clinical FSP, you'll work closely with cross-functional study teams, you will contribute to the coordination, maintenance, and oversight of essential clinical trial documentation and processes, ensuring compliance with regulatory requirements and project timelines.
Key responsibilities
- Support the management and maintenance of study documentation and tracking systems.
- Ensure accuracy, completeness, and quality of clinical trial records throughout the study lifecycle.
- Collaborate with clinical operations teams to coordinate study-related activities and communications.
- Assist with document preparation, filing, archiving, and quality control activities.
- Contribute to compliance with applicable regulatory requirements, SOPs, and Good Clinical Practice (GCP).
- Provide guidance and support to junior team members when appropriate.
- Participate in process improvement initiatives aimed at enhancing operational efficiency.
What You'll Bring
- Previous experience in a Clinical Trial Assistant, Clinical Research Coordinator, Study Coordinator, or similar clinical research support role.
- Minimum 2 years of experience within clinical research.
- Solid organizational and document management skills.
- Strong attention to detail and ability to manage multiple priorities.
- Excellent communication skills in Dutch and English.
- Good knowledge of Microsoft Office applications.
- Understanding of ICH-GCP and clinical research processes.
Build Your Future with IQVIA
If you are looking to build a career in clinical research and want to contribute to studies that improve patient outcomes worldwide, we would love to hear from you. As a Clinical Trial Assistant within Clinical FSP, you will play an important role in supporting the successful execution of clinical trials while developing valuable skills and experience within a global organization dedicated to transforming healthcare through human science and data science.
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.