Description
IQVIA Netherlands is seeking a motivated Clinical Research Associate I practitioner to join our unique and dynamic Sponsor dedicated model.
As a Clinical Research Associate I, you will perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, administer protocol and related study training, evaluate study site practices, manage study progress, and ensure compliance with regulatory requirements.
Responsibilities:
- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Work with sites to adapt, drive, and track subject recruitment plans
- Administer protocol and related study training to assigned sites
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure copies of site documents are available for filing in the Trial Master File
- Create and maintain documentation regarding site management and monitoring visit findings
- Collaborate with study team members for project execution support
Profile:
- Bachelor's Degree in a scientific discipline or healthcare
- Minimum of 6 months of independent, on-site monitoring experience within a CRO or pharmaceutical environment
- Full professional fluency in both Dutch (minimum C1 level) and English
- Good knowledge of applicable clinical research regulatory requirements
- Organizational and problem-solving skills
- Exceptional interpersonal and cross-cultural communication skills
What we offer:
- Choice of company car or flexible mobility allowance
- Premium technology bundle
- Strong focus on career advancement
- Home office setup support and annual wellness reimbursement
- Comprehensive time-off policy
- Premium benefits package