Regulatory Compliance Specialist
2 weeks ago
About this Role
ResponsibilitiesThis Clinical Research Associate position is responsible for ensuring the successful conduct of clinical trials at study sites.
Key Responsibilities
- Conduct site monitoring visits to ensure compliance with GCP and ICH guidelines.
- Develop and implement subject recruitment plans with study sites.
- Provide protocol training and maintain regular communication with sites.
- Assess the quality and integrity of study site practices.
- Monitor study progress through tracking regulatory submissions and approvals.
Requirements
- High school diploma or equivalent degree in a scientific field or healthcare.
- Familiarity with clinical research regulations and therapeutic areas.
- Excellent communication and organizational skills.
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