Senior Clinical Research Associate
On-siteUtrecht, Utrecht, The Netherlands
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams for accurate data collection, while training site staff to maintain high conduct standards. Build effective relationships with site personnel and stakeholders to facilitate smooth trial operations. This role requires fluency in Dutch and English, with a strong foundation in clinical trial monitoring and independent site management. The position is sponsored and offers a competitive total rewards package including health, dental, vision, and retirement plans. Join ICON Strategic Solutions to oversee global healthcare intelligence and bring new medicines to patients faster.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices
- Data integrity
- Site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Fluency in Dutch
- Fluency in English
- Legal right to work in the country where the role is based
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