Clinical Research Assistant
hace 2 meses
About the Role
We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team. As a Clinical Trial Coordinator, you will provide administrative and technical support to our project teams, ensuring seamless execution and compliance with regulatory requirements.
Key Responsibilities
- Coordinate and oversee trial activities, ensuring timely completion and high-quality standards
- Perform file reviews, document findings, and maintain study-related documentation
- Provide system support, including GoBalto and eTMF
- Support Risk-Based Monitoring activities and administrative tasks
- Review and track local regulatory documents, transmit documents to clients, and analyze study metrics
Requirements
- High school diploma or equivalent, with a Bachelor's degree preferred
- Previous experience in clinical trials or a related field, with a strong understanding of ICH GCP and regulatory requirements
- Excellent organizational skills, attention to detail, and ability to work independently or as part of a team
- Strong communication and customer focus, with proficiency in MS Office and clinical trial database systems
What We Offer
At PPD, we value our employees' health and wellbeing. We offer a competitive compensation package, including benefits focused on employee health and wellbeing, as well as opportunities for career advancement and professional growth.
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