Jobid: 3197638480 (0.11)
Overview
As a Clinical Research Associate with IQVIA, you support sponsor-dedicated trials within the CFSP model, gaining exposure to leading pharma and biotech programs. You will monitor multiple investigational sites across therapeutic areas and collaborate with cross-functional teams to ensure patient safety, data integrity, and study quality. The role blends hands-on site monitoring with ongoing mentorship and structured development within a global clinical research environment. This is an opportunity to shape trial delivery while advancing your career in a supportive, flexible setting.
Arbeidsvoorwaarden / Benefits
- car with private use or mobility allowance
- learning and development resources
- home office setup support
- annual wellness reimbursement
- leave policy with annual vacation days and additional year-end leave
- pension plan and multiple insurances
Verantwoordelijkheden
- Conduct site qualification, initiation, monitoring, and close-out visits per protocol and regulatory standards
- Ensure SIHas patient safety, data integrity, protocol compliance, and study quality
- Build and maintain relationships with investigators and site staff, providing training and support
- Monitor study progress, regulatory documentation, patient recruitment, data queries, and site performance metrics
- Collaborate with sites to optimize patient recruitment and retention to meet timelines
- Maintain inspection-ready study documents (ISF, TMF, monitoring reports, follow-ups)
- Identify and escalate risks and quality concerns with timely resolution
- Partner with cross-functional study teams to support study execution and objectives
- Mentor g junior clinical team members through coaching and co-monitoring
- Contribute to continuous improvement and support start-up, maintenance, close-out, and site financial activities
Belangrijkste vereisten
- 1.5 years of on-site monitoring experience in CRO/pharma/biotech/healthcare
- Strong knowledge of GCP and ICH guidelines and regulatory requirements
- Preferrable experience in sponsor-dedicated or CFSP environment
- Knowledge of patient recruitment and start-up activities preferred
- Excellent communication, organizational, and stakeholder management skills
- Fluent Dutch (C1) and English; strong written and verbal communication
- Ability to work independently, manage multiple priorities, and collaborate cross-functionally
- Willingness to travel within the region (about 40%) and hold a Class B driver’s license
- excellent communication
- organizational skills
- stakeholder management
- GCP
- ICH guidelines
- regulatory compliance
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