Clinical Research Jobs At IQVIA Netherlands
Are you searching for Clinical Research Jobs in Europe with a global healthcare leader? This Site Research Assistant role in Utrecht offers an excellent job opportunity for life science graduates looking to gain hands-on experience in clinical trials. Join IQVIA Careers in the Netherlands and play a vital role in supporting clinical research that improves patient outcomes worldwide.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The company creates intelligent connections that accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide.
Job Details
- Job Title: Site Research Assistant – Utrecht
- Location: Utrecht, Netherlands
- Employment Type: Part-time
- Work Model: Field-based
- Hours: 16 hours per week
- Contract Duration: Approximately 6 months
- Job ID: R1528478
Clinical Research Job Role Overview
IQVIA is recruiting a Site Research Assistant / Clinical Research Coordinator to support a clinical research site in Utrecht. This role has an immediate start and involves providing operational and administrative support to a clinical research study under the direction of the Principal Investigator.
The Site Research Assistant plays a key role in maintaining a safe study environment in accordance with health and safety policies and ensuring the smooth execution of the clinical trial.
Key Responsibilities
- Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and related study files
- Support patient screening and enrolment activities, including collection of informed consent and privacy documentation
- Plan and coordinate logistical activities for study procedures in line with the study protocol
- Perform data entry, data quality checks, and query resolution to ensure protocol adherence and data accuracy
- Manage and coordinate shipment of biological samples
- Liaise with study monitors regarding study-related issues and respond to monitor-initiated queries
- Perform general administrative research tasks to support the clinical trial team
Candidate Requirements
- Bachelor’s degree (BS/BA) in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting
- At least 1–2 years of experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
- Good knowledge of clinical trials, including departmental, protocol-specific, and study-specific procedures, consent forms, and schedules
- Basic knowledge of medical terminology
- Strong IT skills, including proficiency with MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word)
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships
- Strong organizational skills with high attention to detail
- Fluency in Dutch
