Freelance Clinical Research Associate - job 1 of 2
Skills
- Strong knowledge of GCP/ICH Guidelines
- Fluency in English and Dutch
- Proficiency in Microsoft Office
Responsibilities
- Conducts site evaluations and initiates visits
- Performs training for site staff
- Conducts periodic monitoring visits
- Manages investigational products and trial materials
- Ensures compliance with protocol and regulatory guidelines
Education
- University Degree in scientific medical or paramedical disciplines
Benefits
- Flexibility of freelance work
- Opportunities for professional development
- Supportive work culture
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