Clinical Research Associate
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Job Description
Clinical Research Associate ensuring compliance and quality in clinical trials. Conducting site monitoring visits and collaborating with teams to maintain trial standards.
Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits)
- Collaborate with cross-functional teams and CRAs to maintain high standards of clinical trial conduct
- Conduct investigational product (IP) inventory and accountability
- Consistently prepares accurate monitoring visit reports and communication logs
- Assists in CRA new hire training and onboarding
Requirements:
- Bachelor’s degree in a relevant field (sciences, nursing, medical preferred)
- Preferred 5+ years’ experience in the clinical research or health care fields
- Clinical monitoring experience in the pharmaceutical, biotech, medtech or CRO industries
- Expertise in data management, site management and monitoring
- Strong command of English, and the local language as necessary, both written and verbal.
Benefits:
- Health insurance
- Professional development
- Global travel
- Flexible work programs
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