Clinical Research Associate
il y a 6 jours
**Job description**:
- Responsible for relationship building and management and maintain regular communications with investigator sites
- Act as the main point of contact for all site
- and study-level questions
- Responsible for site and monitoring quality, regulatory and GCP compliance
- Conduct and report oversight activities, both remote and onsite visits
- Accountable for identifying site and CRA performance issues and quality issues, escalating and supporting implementation of CAPAs to address these
- Review of monitoring visit reports and serve as key contributor to process improvement initiatives
**Benefits**:
- Challenging projects based on your interests and skills
- Personal follow-up and clear, transparent communication both before and after commencement of employment
- Possibility to follow extra training
- Inspiring network events and legendary after work drinks
- Strong network of industry leading clients
- Expertise within IT, Engineering and Life Sciences
- A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
**Have you got what it takes?**:
- A scientific or technical degree in the healthcare area is preferred
- At least a first experience in Clinical Research
- Site Management/Monitoring experience is preferred
- English, French and Dutch are required
Reference number: 46794
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