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Clinical Research Coordinator
2 months ago
We are seeking a highly skilled and experienced Clinical Research Associate (CRA) to join our team at Albion Rye Associates. As a CRA, you will play a critical role in the success of our clinical trials, working closely with our team to ensure the smooth execution of projects.
Key Responsibilities- Monitoring and Managing Clinical Trials: Conduct site monitoring visits to ensure compliance with regulatory requirements and study protocols.
- Project Oversight: Oversee projects from initiation to closeout, ensuring timely and budget-friendly delivery.
- Collaboration and Communication: Liaise with sponsors, vendors, and internal teams to ensure seamless project execution.
- eTMF Management: Manage and maintain electronic Trial Master Files (eTMFs) to ensure accurate and up-to-date documentation.
- Training and Development: Develop training materials and provide training to colleagues to ensure knowledge sharing and skill enhancement.
- Education: Bachelor's degree in science or life sciences.
- Experience: Minimum 3 years of CRA experience, with Phase I experience preferred.
- Skills: Proficiency in eTMF software and excellent communication and project management skills.